Compositions and formulations including cabazitaxel and human serum albumin

ABSTRACT

This document relates to non-covalently bound complexes comprising cabazitaxel and human serum albumin. This document also relates to compositions comprising non-covalently bound complexes comprising cabazitaxel and human serum albumin. This document also relates to compositions comprising cabazitaxel and human serum albumin. This document also relates to compositions consisting essentially of cabazitaxel and human serum albumin.

CLAIM OF PRIORITY

This application claims the benefit of U.S. provisional application No.62/420,986 filed Nov. 11, 2016, and U.S. provisional application No.62/279,074 filed Jan. 15, 2016.

The entire contents of the foregoing are hereby incorporated byreference.

TECHNICAL FIELD

This document relates to complexes and compositions for the treatment ofproliferative diseases.

BACKGROUND

Many drugs for parenteral use are insoluble in water, and are thusformulated with solubilizing agents, surfactants, solvents, and/oremulsifiers that are irritating, allergenic, or toxic when administeredto patients. See, e.g., Briggs et al., Anesthesis 37, 1099 (1982), andWaugh et al., Am. J. Hosp. Pharmacists, 48, 1520 (1991)). Further, manyof these drugs, especially those administered intravenously, causeundesirable side effects such as venous irritation, phlebitis, burningand pain on injection, venous thrombosis, extravasation, and otheradministration related side effects. Additionally, often free drugspresent in formulations induce pain or irritation upon administration.

Taxanes play an important role in the treatment of various solid tumors.Cabazitaxel (trade name Jevtana®) is a semi-synthetic taxane derivative.It was developed by Sanofi-Aventis and was approved by the U.S. FDA forthe treatment of hormone-refractory prostate cancer on Jun. 17, 2010.Cabazitaxel in combination with prednisone is a treatment option forhormone-refractory prostate cancer following cabazitaxel-basedtreatment. JEVTANA is supplied as a kit consisting of (a) a JEVTANAinjection, which contains 60 mg cabazitaxel in 1.5 mL polysorbate 80;and (b) a diluent, containing approximately 5.7 mL 13% (W/W) ethanol.Prior to administration, the JEVTANA injection must first be mixed withthe diluent, which dilutes the amount of Cabazitaxel to 10 mg/mL, andthen further diluted with either 0.9% sodium chloride solution or 5%dextrose solution for infusion. See JEVTANA Prescribing Information.

Other taxane compounds include cabazitaxel, which is marketed asTaxotere® and is FDA-approved for breast cancer, non-small cell lungcancer, hormone refractory prostate cancer, gastric adenocarcinoma, andsquamous cell carcinoma of head and neck cancer. The clinicalintravenous administration of commercially available cabazitaxel(Taxotere®) is formulated in a highly concentrated solution containing40 mg cabazitaxel and 1040 mg Polysorbate 80 per mL. See TAXOTEREPrescribing Information.

The presence of polysorbate 80 in JEVTANA, as well as TAXOTERE, canresult in serious side effects. It has been reported that cabazitaxeladministration is associated with the occurrence of unpredictable(acute) hypersensitivity reactions and cumulative fluid retention. See,e.g., Trudeau M E et al., J Clin Oncol 1996; 14:422-8, Piccart M J etal., J Natl Cancer Inst 1995; 87:676-81, Bruno R et al., J Clin Oncol1998; 16:187-96. These side-effects have been attributed, in part, tothe presence of polysorbate 80.

In order to reduce the side effects induced by polysorbate 80, patientsmay be treated with dexamethasone prior to each dose of JEVTANA.Dexamethasone is a steroid that suppresses the immune response inpatients, which can be especially detrimental in cancer patients underchemotherapy, whose immunity may already be compromised due to thedestruction of healthy cells by the chemotherapeutic treatment. As aresult, these patients can be susceptible to bacterial and fungalinfections. Further, despite receiving the dexamethasone pre-medication,patients can report hypersensitivity side effects from the taxanecompound treatment. Due to these side effects, patients may stop taxanecompound therapy, skip a dose, or continue further therapy at a reduceddose.

Therefore, new formulations of cabazitaxel or other taxane compounds areneeded to avoid these side effects, pre-medication requirements, andpatient noncompliance issues associated with the currently marketedformulation.

SUMMARY

Provided herein are non-covalently bound complexes comprisingcabazitaxel and human serum albumin, e.g., non-covalently boundcomplexes prepared by a process of contacting (e.g., mixing, e.g., in asolution such as an aqueous solution) cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin used toprepare the non-covalently bound complexes are in a ratio by weight fromabout 1:10 to about 1:3000.

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin is afatty acid free human serum albumin. In some embodiments, the humanserum albumin is essentially fatty acid free.

Also, provided herein is a composition comprising non-covalently boundcomplexes comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:10 to about 1:3000. In some embodiments, the pHof the composition is neutral (e.g., pH of the composition is from about5 to about 8, from about 5.5 to about 7.5, or from about 6 to about 7,or the pH of the composition is about 5, about 5.5, about 6, about 6.1,about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, about6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4,about 7.5, or about 8). In some embodiments, the human serum albumin isessentially fatty acid free.

In some embodiments, the composition is a solid formulation. Forexample, the solid formulation can be produced in a uniform manner bylyophilization. A skilled artisan would recognize other methods, such asrotary evaporation, that can also produce solid formulations.

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water. In some embodiments, the aqueousformulation includes water and water-miscible organic solvents includingat least one of polyethylene glycol 300, polyethylene glycol 400,ethanol, methanol, propylene glycol, glycerin, N-methyl-2-pyrrolidone,dimethylacetamide, and dimethylsulfoxide. For example, thewater-miscible organic solvent can include ethanol. In some embodiments,the aqueous formulation includes water and ethanol. In some embodiments,the water-miscible organic solvent can be a mixture of water-miscibleorganic solvents.

In some embodiments, the aqueous formulation is a clear aqueoussolution. In some embodiments, the aqueous formulation is a clearaqueous solution for at least 6 hours. For example, the formulation canbe a clear and stable aqueous solution reconstituted from a sterilelyophilized powder. In some embodiments, the aqueous formulation is aclear aqueous solution, wherein the aqueous formulation is substantiallyfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationis free of solvent other than water.

Also, provided herein is a pharmaceutical composition comprising thenon-covalently bound complexes or the composition comprising thenon-covalently bound complexes of the cabazitaxel and the human serumalbumin as described herein, and a pharmaceutically acceptable carrier.

Also, provided herein is a method of treating a cancer, the methodcomprising the step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising non-covalently bound complexes or the composition comprisingthe cabazitaxel and the human serum albumin as described herein, and apharmaceutically acceptable carrier.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising non-covalently bound complexes or the composition comprisingthe cabazitaxel and the human serum albumin as described herein,prednisone, and a pharmaceutically acceptable carrier.

Also, provided herein is a composition comprising cabazitaxel and humanserum albumin, wherein the cabazitaxel and the human serum albumin inthe composition have a ratio by weight from about 1:10 to about 1:3000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the composition has asolubility in an aqueous solution of at least 10 mg/mL. In someembodiments, the pH of the composition is neutral (e.g., pH of thecomposition is from about 5 to about 8, from about 5.5 to about 7.5, orfrom about 6 to about 7, or the pH of the composition is about 5, about5.5, about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, about 7.5, or about 8).

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin is afatty acid free human serum albumin. In some embodiments, the humanserum albumin is essentially fatty acid free.

In some embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 24 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 3 days when the composition is dissolved in an aqueous solvent. Insome embodiments, the aqueous solution is substantially free of solventother than water. In some embodiments, the aqueous solution is free ofsolvent other than water.

In some embodiments, the composition is a solid formulation. Forexample, the solid formulation can be produced in a uniform manner bylyophilization. A skilled artisan would recognize other methods, such asrotary evaporation, that can also produce solid formulations.

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water.

In some embodiments, the aqueous formulation can be free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80.

In some embodiments, the aqueous formulation is a clear aqueoussolution. For example, the formulation can be a clear and stable aqueoussolution reconstituted from a sterile lyophilized powder. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation is substantially free of solvent otherthan water. In some embodiments, the aqueous formulation is a clearaqueous solution, wherein the aqueous formulation is free of solventother than water.

Also, provided herein is a pharmaceutical composition comprising thecomposition comprising the cabazitaxel and the human serum albumin asdescribed herein, and a pharmaceutically acceptable carrier.

Also, provided herein is a method of treating a cancer, the methodcomprising the step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, prednisone, and a pharmaceuticallyacceptable carrier.

Also, provided herein is a composition consisting essentially ofcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:10 to about 1:3000. In some embodiments, the pH of the composition isneutral (e.g., pH of the composition is from about 5 to about 8, fromabout 5.5 to about 7.5, or from about 6 to about 7, or the pH of thecomposition is about 5, about 5.5, about 6, about 6.1, about 6.2, about6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9,about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, orabout 8).

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin is afatty acid free human serum albumin. In some embodiments, the humanserum albumin is essentially fatty acid free.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent. In some embodiments,the aqueous solution is substantially free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 24 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 3 days when the composition is dissolved in an aqueous solvent. Insome embodiments, the aqueous solution is substantially free of solventother than water.

In some embodiments, the composition is a solid formulation. In someembodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof a surfactant, such as CREMOPHOR® surfactants and Polysorbate 80. Insome embodiments, the aqueous formulation is a clear aqueous solution.

Also, provided herein is a pharmaceutical composition comprising thecomposition consisting essentially of the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

Also, provided herein is a method of treating cancer comprising the stepof administering to a subject in need thereof a therapeuticallyeffective amount of a pharmaceutical composition comprising thecomposition consisting essentially of the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition consisting essentially of the cabazitaxel andthe human serum albumin as described herein, prednisone, and apharmaceutically acceptable carrier.

Also, provided herein is a composition comprising cabazitaxel and humanserum albumin, wherein the cabazitaxel and the human serum albumin inthe composition have a ratio by weight from about 1:100 to about 1:3000.In some embodiments, the pH of the composition is neutral (e.g., pH ofthe composition is from about 5 to about 8, from about 5.5 to about 7.5,or from about 6 to about 7, or the pH of the composition is about 5,about 5.5, about 6, about 6.1, about 6.2, about 6.3, about 6.4, about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1,about 7.2, about 7.3, about 7.4, about 7.5, or about 8).

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin isessentially fatty acid free.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent. In some embodiments,the aqueous solution is substantially free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution for atleast 3 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 24 hours when the composition is dissolved in an aqueous solvent.In some embodiments, the composition is a clear aqueous solution for atleast 3 days when the composition is dissolved in an aqueous solvent. Insome embodiments, the aqueous solution is substantially free of solventother than water.

In some embodiments, the composition is a solid formulation. In someembodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof a surfactant, such as CREMOPHOR® surfactants and Polysorbate 80. Insome embodiments, the aqueous formulation is a clear aqueous solution.

Also, provided herein is a pharmaceutical composition comprising thecomposition comprising the cabazitaxel and the human serum albumin asdescribed herein, and a pharmaceutically acceptable carrier.

Also, provided herein is a method of treating cancer comprising the stepof administering to a subject in need thereof a therapeuticallyeffective amount of a pharmaceutical composition comprising thecomposition comprising the cabazitaxel and the human serum albumin asdescribed herein, and a pharmaceutically acceptable carrier.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, prednisone, and a pharmaceuticallyacceptable carrier.

Also, provided herein is a composition consisting essentially of humanserum albumin and non-covalently bound complexes of cabazitaxel andhuman serum albumin, wherein the cabazitaxel and the human serum albuminin the composition have a ratio by weight from about 1:10 to about1:3000.

Also, provided herein is a composition comprising non-covalently boundcomplexes consisting essentially of cabazitaxel and human serum albumin,wherein the cabazitaxel and the human serum albumin in the compositionhave a ratio by weight from about 1:10 to about 1:3000.

DETAILED DESCRIPTION

Provided herein are non-covalently bound complexes comprisingcabazitaxel and human serum albumin, e.g., non-covalently boundcomplexes prepared by a process of contacting (e.g., mixing, e.g., in asolution such as an aqueous solution) cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin used toprepare the non-covalently bound complexes are in a ratio by weight fromabout 1:10 to about 1:3000.

Also, provided herein is a composition comprising a non-covalently boundcomplex comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:10 to about 1:3000.

Also, provided herein is a composition comprising a non-covalently boundcomplex comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the complex have a ratio byweight from about 1:10 to about 1:3000.

In some embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:2000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:220 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight of about 1:200, 1:210, 1:220, about1:230, about 1:240, about 1:250, about 1:260, about 1:270, about 1:280,about 1:290, about 1:300, about 1:310, about 1:320, about 1:330, about1:340, about 1:350, about 1:360, about 1:370, about 1:380, about 1:390,about 1:400, about 1:450, about 1:460, about 1:500 or about 1:600.

In some embodiments, the non-covalent interaction between cabazitaxeland human serum albumin in the complex comprises hydrogen bonding. Insome embodiments, the non-covalent interaction between cabazitaxel andhuman serum albumin in the complex comprises electrostatic interaction.In some embodiments, the non-covalent interaction between cabazitaxeland human serum albumin in the complex comprises hydrophobicinteraction. In some embodiments, the non-covalent interaction betweencabazitaxel and human serum albumin in the complex comprises Van derWaals forces. In some embodiments, the non-covalent interaction betweencabazitaxel and human serum albumin in the complex comprises hydrogenbonding, electrostatic interaction, hydrophobic interactions and Van derWaals forces.

In some embodiments, the non-covalent interaction between cabazitaxeland human serum albumin in the composition comprises hydrogen bonding.In some embodiments, the non-covalent interaction between cabazitaxeland human serum albumin in the composition comprises electrostaticinteraction. In some embodiments, the non-covalent interaction betweencabazitaxel and human serum albumin in the composition compriseshydrophobic interaction. In some embodiments, the non-covalentinteraction between cabazitaxel and human serum albumin in thecomposition comprises Van der Waals forces. In some embodiments, thenon-covalent interaction between cabazitaxel and human serum albumin inthe composition comprises hydrogen bonding, electrostatic interaction,hydrophobic interactions and Van der Waals forces.

As used herein, the term “human serum albumin” refers to native andrecombinant human serum albumin. Native human serum albumin and otherplasma proteins can be precipitated from human plasma by varying the pHand adding ethanol, in what is known as the Cohn fractionation process(Cohn E J et al., J. Am. Chem. Soc. 1946; 68:459-475). By controllingthe pH and ethanol content, semi-purified fractions of plasma proteinscan be produced. One of the last proteins to precipitate in the Cohnprocess is native human serum albumin. After precipitation, a wet pasteof crude native human serum albumin is obtained. Subsequentbioprocessing steps (purification, filtration, pasteurization, etc.) canbe used to produce a purified, stabilized form of native human serumalbumin for commercial use (Lin J J et al., Pharmaceutical Research2000; 17:391-6). Recombinant human serum albumin is a highly purifiedanimal-, virus-, and prion-free product as alternative to native humanserum albumin, to which it is structurally equivalent (Bosse D et al.,J. Clin. Pharmacol. 2005; 45:57-67). Recombinant human serum albumin hasbeen produced by various hosts, both prokaryotic and eukaryotic (Chen Zet al., Biochimica et Biophysica Acta 2013; 1830:5515-5525). A fattyacid free human serum albumin can be prepared by treatment of humanserum albumin with charcoal at low pH. Likewise, treatment of humanserum albumin with charcoal at low pH can be used to remove fatty acidsfrom human serum albumin (Chen R F, J. Biol. Chem. 1967; 242:173-181).

Human serum albumin (HSA) is a highly soluble globular protein of M_(r)65K and consists of 585 amino acids. HSA is the most abundant protein inthe plasma and accounts for 70-80% of the colloid osmotic pressure ofhuman plasma. The amino acid sequence of HSA contains a total of 17disulphide bridges, one free thiol (Cys 34), and a single tryptophan(Trp 214). Intravenous use of HSA solution has been indicated for theprevention and treatment of hypovolumic shock (see, e.g., Tullis, JAMA,237, 355-360, 460-463, (1977)) and Houser et al., Surgery, Gynecologyand Obstetrics, 150, 811-816 (1980)) and in conjunction with exchangetransfusion in the treatment of neonatal hyperbilirubinemia (see, e.g.,Finlayson, Seminars in Thrombosis and Hemostasis, 6, 85-120, (1980)).

Human serum albumin (HSA) has multiple hydrophobic binding sites (atotal of seven for medium and long-chain fatty acids, an endogenousligand of HSA) and binds a diverse set of drugs, especially neutral andnegatively charged hydrophobic compounds (Goodman et al., ThePharmacological Basis of Therapeutics, 9th ed, McGraw-Hill New York(1996)). Two high affinity binding sites have been proposed insubdomains IIA and IIIA of HSA, which are highly elongated hydrophobicpockets with charged lysine and arginine residues near the surface whichfunction as attachment points for polar ligand features (see, e.g.,Fehske et al., Biochem. Pharmcol., 30, 687-92 (1981), Vorum, Dan. Med.Bull., 46, 379-99 (1999), Kragh-Hansen, Dan. Med Bull., 1441, 131-40(1990), Curry et al., Nat. Struct. Biol., 5, 827-35 (1998), Sugio etal., Protein. Eng., 12, 439-46 (1999), He et al., Nature, 358, 209-15(1992), and Carter et al., Adv. Protein. Chem., 45, 153-203 (1994)).

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin is afatty acid free human serum albumin. In some embodiments, the humanserum albumin is essentially fatty acid free. In some embodiments, thehuman serum albumin contains no more than two moles of fatty acids boundto one mole of human serum albumin. In some embodiments, the human serumalbumin contains no more than one mole of fatty acids bound to one moleof human serum albumin. In some embodiments, human serum albumincontains no more than 0.5 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.1 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.05 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.01 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.001 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0005 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0001 moles of fatty acids bound to one mole ofhuman serum albumin.

As used herein, the term “non-covalently bound complex” refers to acomplex in which the bonds between the components of the complex arenon-covalent bonds (e.g., weak bonds such as hydrogen bonds,electrostatic effects, i-effects, hydrophobic effects and Van der Waalsforces). Further, human serum albumin (HSA) has multiple hydrophobicbinding sites (a total of seven for medium and long-chain fatty acids,an endogenous ligand of HSA) and binds a diverse set of drugs,especially neutral and negatively charged hydrophobic compounds (Goodmanet al., The Pharmacological Basis of Therapeutics, 9th ed, McGraw-HillNew York (1996)). Additionally, after the drug molecule binds to HSA,the drug molecule and HSA form a non-covalently bound drug and proteincomplex through the binding sites of HSA. This concept is commonlyunderstood by one of ordinary skill in the art to which this disclosurebelongs. One example of a non-covalently bound complex is anon-covalently bound complex of HSA and fatty acids, in which the fattyacids bind to HSA through HSA's multiple binding sites.

As used herein, the term “stable” refers to non-covalently boundcomplexes that do not readily disassociate and aggregate into theirseparate parts, e.g., do not readily dissociate and aggregate for aperiod of time of greater than 6 hours, 12 hours, 24 hours, or 3 days).For example, a solution including stable non-covalently bound complexeswill often appear transparent whereas a solution including unstablenon-covalently bound complexes will appear translucent or cloudy.Further, it will be appreciated by those of ordinary skill in the art,that after a period of time, stable non-covalently bound complexes candisassociate and aggregate into their separate parts. Thus, a solutionincluding stable non-covalently bound complexes can become translucentor cloudy after a period of time (e.g., 6 hours, 12 hours, 24 hours, or3 days).

In vitro, the binding of cabazitaxel to human serum proteins was 89 to92% and was not saturable up to 50,000 ng/mL, which covers the maximumconcentration observed in clinical trials. Cabazitaxel is mainly boundto human serum albumin (82%). See JEVTANA Prescribing Information.

As used herein, the term “essentially fatty acid free” refers toproteins (e.g. serum albumin) that contain less than about 0.02% fattyacid by weight. For example, human serum albumin that is essentiallyfatty acid free can contain less than 0.02% fatty acid by weight.

As used herein, the term “fatty acids” refers to non-esterified fattyacids (e.g. linoleic acid, α-linoleic acid, γ-linoleic acid).

As used herein the term cabazitaxel is a compound that has the CAS No.183133-96-2 and the following chemical structure:

Cabazitaxel is lipophilic, practically insoluble in water and soluble inalcohol.

Further, cabazitaxel is a microtubule inhibitor indicated in combinationwith prednisone for treatment of patients with hormone-refractorymetastatic prostate cancer previously treated with acabazitaxel-containing treatment regimen.

In some embodiments, the cabazitaxel can be a pharmaceuticallyacceptable salt of cabazitaxel.

As used herein, the term “pharmaceutically acceptable salts” refers tosalts that retain the desired biological activity of the subjectcompound and exhibit minimal undesired toxicological effects. Thesepharmaceutically acceptable salts may be prepared in situ during thefinal isolation and purification of the compound, or by separatelyreacting the purified compound in its free acid or free base form with asuitable base or acid, respectively. In some embodiments,pharmaceutically acceptable salts may be preferred over the respectivefree base or free acid because such salts impart greater stability orsolubility to the molecule thereby facilitating formulation into adosage form. Basic compounds are generally capable of formingpharmaceutically acceptable acid addition salts by treatment with asuitable acid. Suitable acids include pharmaceutically acceptableinorganic acids and pharmaceutically acceptable organic acids.Representative pharmaceutically acceptable acid addition salts includehydrochloride, hydrobromide, nitrate, methylnitrate, sulfate, bisulfate,sulfamate, phosphate, acetate, hydroxyacetate, phenylacetate,propionate, butyrate, isobutyrate, valerate, maleate, hydroxymaleate,acrylate, fumarate, malate, tartrate, citrate, salicylate,p-aminosalicyclate, glycollate, lactate, heptanoate, phthalate, oxalate,succinate, benzoate, o-acetoxybenzoate, chlorobenzoate, methylbenzoate,dinitrobenzoate, hydroxybenzoate, methoxybenzoate, mandelate, tannate,formate, stearate, ascorbate, palmitate, oleate, pyruvate, pamoate,malonate, laurate, glutarate, glutamate, estolate, methanesulfonate(mesylate), ethanesulfonate (esylate), 2-hydroxyethanesulfonate,benzenesulfonate (besylate), p-aminobenzenesulfonate, p-toluenesulfonate(tosylate), napthalene-2-sulfonate, ethanedisulfonate, hydrogenbisulfide, bitartrate, gluconate, glucuronate,para-bromophenylsulfonate, carbonate, pyrosulfate, sulfite, bisulfite,monohydrogen phosphate, dihydrogen phosphate, metaphosphate,pyrophosphate, chloride, bromide, iodide, decanoate, caprylate, caprate,propiolate, suberate, sebacate, butyne-1,4-dioate, hexyne-1,6-dioate,terephthalate, sulfonate, xylenesulfonate, phenylpropionate,phenylbutyrate, β-hydroxybutyrate, glycolate, propanesulfonate,naphthalene-1-sulfonate, naphthalene-2-sulfonate and2,5-dihydroxybenzoate. Suitable bases include pharmaceuticallyacceptable inorganic bases and pharmaceutically acceptable organicbases. Representative pharmaceutically acceptable base addition saltsinclude hydroxide of alkali metals including sodium, potassium, andlithium; hydroxides of alkaline earth metals such as calcium andmagnesium; hydroxides of other metals, such as aluminum and zinc;ammonia, organic amines such as unsubstituted or hydroxyl-substitutedmono-, di-, or tri-alkylamines, dicyclohexylamine; tributyl amine;pyridine; N-methyl, N-ethylamine; diethylamine; triethylamine; mono-,bis-, or tris-(2-OH—(C₁-C₆)-alkylamine), such asN,N-dimethyl-N-(2-hydroxyethyl)amine or tri-(2-hydroxyethyl)amine;N-methyl-D-glucamine; morpholine; thiomorpholine; piperidine;pyrrolidine; and amino acids such as arginine, lysine, and the like.

In some embodiments, the cabazitaxel can be a cabazitaxel with oneequivalent of the acetone solvate. In some embodiments, cabazitaxel, ora salt thereof, may be crystalline or amorphous. In some embodiments,cabazitaxel, or a salt thereof, may be in a form of a hydrate. In someembodiments, the cabazitaxel can be any one of cabazitaxel solvates,hydrates, and/or crystal forms disclosed, for example, in US applicationpublication No. 20150315164, US application publication No. 20160257663,US application publication No. 20160340327, US application publicationNo. 20160244420, US application publication No. 20150141673, U.S. Pat.Nos. 9,012,665, 9,353,076, 9,394,266, 9,309,210, 9,199,953, 8,735,611,8,735,611, 8,901,322, PCT publication No. WO2014115168, PCT publicationNo. WO2015087228, PCT publication No. WO2014067207, PCT publication No.WO2014128728 or PCT publication No. WO2015058960, the disclosures ofeach of the above are incorporated herein by reference in theirentirety.

Also, provided herein is a composition comprising a non-covalently boundcomplex comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:10 to about 1:3000. In some embodiments, the pHof the composition is neutral (e.g., pH of the composition is from about5 to about 8, from about 5.5 to about 7.5, or from about 6 to about 7,or the pH of the composition is about 5, about 5.5, about 6, about 6.1,about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, about6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4,about 7.5, or about 8).

In some embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:2000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:220 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight of about 1:200, 1:210, 1:220, about1:230, about 1:240, about 1:250, about 1:260, about 1:270, about 1:280,about 1:290, about 1:300, about 1:310, about 1:320, about 1:330, about1:340, about 1:350, about 1:360, about 1:370, about 1:380, about 1:390,about 1:400, about 1:450, about 1:460, about 1:500 or about 1:600.

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin is afatty acid free human serum albumin. In some embodiments, the humanserum albumin is essentially fatty acid free. In some embodiments, thehuman serum albumin contains no more than two moles of fatty acids boundto one mole of human serum albumin. In some embodiments, the human serumalbumin contains no more than one mole of fatty acids bound to one moleof human serum albumin. In some embodiments, human serum albumincontains no more than 0.5 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.1 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.05 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.01 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.001 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0005 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0001 moles of fatty acids bound to one mole ofhuman serum albumin.

In some embodiments, the cabazitaxel can be a pharmaceuticallyacceptable salt of cabazitaxel. In some embodiments, cabazitaxel can beany one of crystal forms, amorphous forms, solvates and hydrates asdescribed herein.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solution. In someembodiments, the aqueous solution is substantially free of solvent otherthan water. In some embodiments, the aqueous solution is free of solventother than water.

As used herein, the term “clear aqueous solution” refers to an aqueoussolution containing cabazitaxel and HSA that is transparent andsubstantially free of visible particles or precipitation of undissolvedcabazitaxel when visually observed. For example, the term “clear aqueoussolution” excludes a milky aqueous solution. Further, the term“transparent aqueous solution” excludes a cloudy or hazy aqueoussolution.

As used herein, the term “substantially free of visible particles orprecipitation of undissolved cabazitaxel” can be assessed as follows:after a clear aqueous solution is filtered with a 0.22 micron filter,the amount of cabazitaxel in the filtered clear aqueous solution is atleast 95% of the total amount of cabazitaxel in the clear aqueoussolution before filtration. The total amount of cabazitaxel in theaqueous solution before filtration includes the particles orprecipitation of undissolved cabazitaxel in the aqueous solution or withthe aqueous solution. The amount of the cabazitaxel in a clear aqueoussolution can be measured by methods using HPLC. The methods of measuringthe amount of the cabazitaxel in a clear aqueous solution areillustrated in the experimental examples described herein. The methodsare commonly understood by one of ordinary skill in the art to whichthis disclosure belongs.

As used herein, the term “micron” refers to a unit of measure of oneone-thousandth of a millimeter. In some embodiments, the term “micron”refers to a micrometer.

As used herein, “substantially free of solvent,” in reference to anaqueous solution, refers to an aqueous solution that contains less than0.5%, by weight, of any non-water solvent. In some embodiments, theaqueous solution contains less than 0.1%, by weight, of any non-watersolvent. In some embodiments, the aqueous solution contains less than0.05%, by weight, of any non-water solvent.

As used herein, the term “aqueous solution” refers to a solution,wherein at least one solvent is water and the weight % of water in themixture of solvents is at least 50%, at least 60%, at least 70% or atleast 90%. In some embodiments, aqueous solution is a solution in whichwater is the only solvent. In some embodiments, aqueous solution is 0.9%saline solution. In some embodiments, aqueous solution is 5% dextrosewater solution. In some embodiments, aqueous solution is a buffer (e.g.,phosphate buffer or a carbonate buffer). In some embodiments, the bufferis physiological buffer or a pharmaceutically acceptable buffer. In someembodiments, the buffer is any one of buffers described, for example, inY.-C. Lee et al. International Journal of Pharmaceutics 253 (2003)111-119, the disclosure of which is incorporated herein by reference inits entirety. In some embodiments, the buffer comprises maleic acid,tartaric acid, lactic acid, citric acid, acetic acid, sodiumbicarbonate, sodium phosphate, or mixtures thereof. In some embodiments,the pH range of the buffer is from about 3 to about 9, from about 4 toabout 8, from about 5 to about 7, from about 6 to about 7, from about 3to about 5, from about 3 to about 7, from about 4 to about 6, or fromabout 6 to about 6. In some embodiments, the pH of the buffer is about4, about 5, about 6, about 6.4, about 6.5, about 6.6, about 7, about7.5, or about 8.

As used herein, the term “aqueous solvent” refer to a liquid comprisingat least 50%, at least 60%, at least 70%, at least 90% or at least 95%water. In some embodiments, aqueous solvent is water.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solvent when the compositionis dissolved in an aqueous solution, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, provided herein is a composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in 0.9% saline. In some embodiments, the composition is aclear aqueous solution when the composition is dissolved in 5% dextrosesolution.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in an aqueous solvent, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7.0, about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous solution is substantially free of solvent otherthan water. In some embodiments, the aqueous solution is free of solventother than water.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in water, wherein the clear aqueoussolution has pH value from about 5 to about 8. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 5.5 to about 7.8. In some embodiments, the composition forms aclear aqueous solution, when the composition is dissolved in water,wherein the clear aqueous solution has pH value from about 6 to about7.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in water, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in water, wherein the clear aqueous solutionhas pH value from about 6 to about 6.5. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 6.5 to about 7. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in water, whereinthe clear aqueous solution has pH value from about 7 to about 7.5. Insome embodiments, the composition forms a clear aqueous solution, whenthe composition is dissolved in water, wherein the clear aqueoussolution has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 0.9% saline, wherein the clearaqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 5.5 to about 7.8. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue from about 6 to about 7.5. In some embodiments, the compositionforms a clear aqueous solution, when the composition is dissolved in0.9% saline, wherein the clear aqueous solution has pH value from about6.5 to about 7.5. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in 0.9% saline,wherein the clear aqueous solution has pH value from about 6 to about6.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in 0.9% saline, wherein theclear aqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 7 to about 7.5. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 5% dextrose solution, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7.0, about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 96% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 98% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99.5% of the total amountof cabazitaxel in the aqueous solution before the filtration. In someembodiments, the aqueous solution is free of solvent other than water.In some embodiments, the aqueous solution is substantially free ofsolvent other than water.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solution, wherein after theclear aqueous solution is filtered by a 0.22 micron filter, the amountof cabazitaxel in the filtered aqueous solution is at least 95%, 96%,97%, 98%, 99%, or 99.5% of the total amount of cabazitaxel in theaqueous solution before the filtration, wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 6 to about 7.5, and wherein the clear aqueoussolution is substantially free of solvent other than water. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 5 to about 8, and wherein the clear aqueous solutionis free of solvent other than water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in an aqueous solution, wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforethe filtration, wherein the clear aqueous solution has pH value fromabout 6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, the amount of cabazitaxel that is bound to the HSA(e.g., non-covalently) in the aqueous solution (e.g., clear aqueoussolution) comprising the composition comprising a non-covalently boundcomplex comprising cabazitaxel and human serum albumin (as describedherein) is at least 40%, at least 50%, at least 60%, at least 70%, atleast 80%, at least 90%, at least 95%, at least 99%, or about 100% ofthe total about of cabazitaxel in the aqueous solution.

In some embodiments, the composition is an aqueous solution, whereinafter the aqueous solution is filtered by a 0.22 micron filter, theamount of cabazitaxel in the filtered aqueous solution is at least 80%of the total amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, the composition is an aqueous solution,wherein after the aqueous solution is filtered by a 0.22 micron filter,the amount of cabazitaxel in the filtered aqueous solution is at least85% of the total amount of cabazitaxel in the aqueous solution beforethe filtration. In some embodiments, the composition is an aqueoussolution, wherein after the aqueous solution is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 90% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, the aqueoussolution is free of solvent other than water. In some embodiments, theaqueous solution is substantially free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution for atleast 1 hour when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 2 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 3 hours when the composition isdissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 4 hours when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the composition is a clear aqueoussolution for at least 5 hours when the composition is dissolved in anaqueous solution (e.g. water, 0.9% saline, or 5% dextrose solution). Insome embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 8 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 24 hours when the compositionis dissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 3 days when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the aqueous solution is substantiallyfree of solvent other than water. In some embodiments, the aqueoussolution is free of solvent other than water.

In some embodiments, the composition is a solid formulation. Forexample, the solid formulation can be produced in a uniform manner bylyophilization. A skilled artisan would recognize other methods, such asrotary evaporation, that can also produce solid formulations.

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water. In some embodiments, the aqueousformulation includes water and water-miscible organic solvents includingat least one of polyethylene glycol 300, polyethylene glycol 400,ethanol, methanol, propylene glycol, glycerin, N-methyl-2-pyrrolidone,dimethylacetamide, and dimethylsulfoxide. For example, thewater-miscible organic solvent can include ethanol. In some embodiments,the aqueous formulation includes water and ethanol. In some embodiments,the water-miscible organic solvent can be a mixture of water-miscibleorganic solvents. In some embodiments, the pH of the aqueous formulation(e.g., clear aqueous solution) is neutral (e.g., pH of the compositionis from about 5 to about 8, from about 5.5 to about 7.5, or from about 6to about 7, or the pH of the composition is about 5, about 5.5, about 6,about 6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about6.7, about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3,about 7.4, about 7.5 or about 8).

In some embodiments, the aqueous formulation can be free of asurfactant. In some embodiments, the aqueous formulation can be free ofa surfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant selected from the group consisting of CREMOPHOR® surfactantsand Polysorbate 80.

As used herein, the term “substantially free of surfactant” refers to aformulation containing less than 0.0005%, less than 0.0003%, or lessthan 0.0001% of surfactants and/or less than 0.0005%, less than 0.0003%,or less than 0.0001% of surfactant.

In some embodiments, the aqueous formulation is a clear aqueoussolution. For example, the formulation can be a clear and stable aqueoussolution reconstituted from a sterile lyophilized powder. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation is substantially free of solvent otherthan water. In some embodiments, the aqueous formulation is a clearaqueous solution, wherein the aqueous formulation is free of solventother than water.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline. In some embodiments, theaqueous formulation is a clear aqueous solution reconstituted from thesolid formulation (e.g. the sterile lyophilized powder) in 5% dextrosesolution.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 5 to about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 5 to about 8.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 5 to about 8. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinthe pH of 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 5 to about 8. In some aspects of theaforementioned embodiments, the concentration of the reconstituted solidin the aqueous formulation is about 25 mg, about 50 mg, about 75 mg,about 100 mg, about 150 mg or 200 mg per 1 mL of the aqueous solvent. Insome aspects of the aforementioned embodiments, the concentration of thereconstituted solid in the aqueous formulation is from about 10 mg toabout 200 mg per 1 mL of the aqueous solvent.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 6 to about 7.5. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinpH of the 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value of about 6, about 6.1, about 6.2, about6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9,about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, orabout 8. In some embodiments, the aqueous formulation is a clear aqueoussolution reconstituted from the solid formulation (e.g. the sterilelyophilized powder) in 0.9% saline solution, wherein the pH of 0.9%saline solution is about 5.4, and wherein the aqueous formulation has pHvalue of about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, about 7.5, or about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose water solution, wherein pH of the 5% dextrose solution is about4.4, and wherein the aqueous formulation has pH value of about 6, about6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7,about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about7.4, about 7.5, or about 8.

In some embodiments, the aqueous formulation has pH value from about 5to about 8. In some embodiments, the aqueous formulation has pH valuefrom about 5.5 to about 7.8. In some embodiments, the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation has pH value from about 6.5 to about 7.5. Insome embodiments, the aqueous formulation has pH value from about 6 toabout 6.5. In some embodiments, the aqueous formulation has pH valuefrom about 6.5 to about 7. In some embodiments, the aqueous formulationhas pH value from about 7 to about 7.5. In some embodiments, the aqueousformulation has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water.

In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 5 toabout 8, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 5 to about 8, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 5.5 to about 7.8, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 5.5 to about7.8, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about7.5, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 6.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 6.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about 7,and wherein the aqueous formulation is free of solvent other than water.In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 7 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 7 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value about 6, about 6.1, about 6.2, about 6.3, about 6.4, about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1,about 7.2, about 7.3, about 7.4, or about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value about 6, about 6.1, about6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8,about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, orabout 7.5, and wherein the aqueous formulation is free of solvent otherthan water.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 95% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 96% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, after the aqueous formulation is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 98% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration. In some embodiments, after the aqueousformulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 99% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 99.5% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is substantially freeof solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is substantially free of solvent other thanwater. In some embodiments, after the aqueous formulation (e.g. a clearaqueous solution) is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before filtration, wherein the clear aqueous solution has pHvalue from about 5 to about 8, and wherein the clear aqueous solution isfree of solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is free of solvent other than water. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 80% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 85% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 90% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, the aqueous formulation is a clear aqueous solutionfor at least 1 hour. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 2 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 4 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 5 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 8 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 24 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours ata concentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is a clear aqueous solution for at least 24 hours. In someembodiments, the aqueous formulation is a transparent aqueous solutionfor at least 24 hours at a concentration of from about 5 mg/mL to about250 mg/mL, from about 10 mg/mL to about 200 mg/mL, from about 25 mg/mLto about 150 mg/mL, from about 10 mg/mL to about 50 mg/mL, from about 50mg/mL to about 100 mg/mL, from about 100 mg/mL to about 150 mg/mL, fromabout 150 mg/mL to about 200 mg/mL, or about 5 mg/mL, about 10 mg/mL,about 20 mg/mL, about 30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60mg/mL, about 70 mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100mg/mL at a temperature from about 1° C. to about 35° C., about 1° C. toabout 10° C., about 10° C. to about 20° C., about 20° C. to about 35°C., or about 1° C., about 5° C., about 10° C., about 15° C., about 20°C., about 25° C., about 30° C., or about 35° C. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 days. Insome embodiments, the aqueous formulation is a transparent aqueoussolution for at least 3 days when dissolved in an aqueous solution at aconcentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is free of solvent other thanwater.

Also, provided herein is a pharmaceutical composition comprising thecomposition comprising a non-covalently bound complex comprisingcabazitaxel and human serum albumin as described herein, and apharmaceutically acceptable carrier.

In some embodiments, the pharmaceutical composition further comprises atleast one anti-cancer drug (e.g., any one of the anti-cancer drugs asdescribed herein).

As used herein, the term “pharmaceutically acceptable carrier” is meantany solution used to solubilize and deliver an agent to a subject. Adesirable pharmaceutically acceptable carrier is saline. Otherpharmaceutically acceptable carrier and their formulation are known toone skilled in the art and described, for example, in Remington'sPharmaceutical Sciences. (20^(th) edition), ed. A. Gennaro, 2003,Lippincon Williams & Wilkins.

Pharmaceutically acceptable carriers that may be used in thepharmaceutical compositions of the present application include, but arenot limited to, ion exchangers, alumina, aluminum stearate, lecithin,serum proteins (other than HSA), buffer substances such as phosphates,glycine, sorbic acid, potassium sorbate, salts or electrolytes, such asprotamine sulfate, disodium hydrogen phosphate, potassium hydrogenphosphate, sodium chloride, zinc salts, colloidal silica, magnesiumtrisilicate, and cellulose-based substances.

Formulations suitable for parenteral administration include aqueous andnon-aqueous, isotonic sterile injection solutions, which can containanti-oxidants, buffers, bacteriostats, and solutes that render theformulation compatible with the blood of the intended recipient, andaqueous and non-aqueous sterile suspensions that can include suspendingagents, solubilizers, thickening agents, stabilizers, and preservatives.The formulations can be presented in unit-dose or multi-dose sealedcontainers, such as ampules and vials, and can be stored in afreeze-dried (lyophilized) condition requiring only the addition of thesterile liquid excipient, for example, water, for injections,immediately prior to use. Extemporaneous injection solutions andsuspensions can be prepared from sterile powders, granules, and tablets.

In some embodiments, the pharmaceutical composition is free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the pharmaceutical composition is substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the pharmaceutical composition can be substantially free ofa surfactant selected from the group consisting of CREMOPHOR®surfactants and Polysorbate 80.

Also, provided herein is a method of treating a proliferative diseasecomprising the step of administering to a subject in need thereof atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising a non-covalently bound complexcomprising cabazitaxel and human serum albumin as described herein, anda pharmaceutically acceptable carrier.

As used herein, the terms “individual”, “patient”, or “subject” are usedinterchangeably and refer to any animal, including mammals, preferablymice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep,horses, or primates, and most preferably humans.

As used herein, the term “proliferative disease” refers to a diseasecaused by excessive proliferation of cells and turnover of cellularmatrix. Non-limiting examples of proliferative diseases include cancer,atherosclerosis, arthritis (e.g. rheumatoid arthritis), psoriasis,fibrosis (e.g. pulmonary fibrosis, idiopathic pulmonary fibrosis),scleroderma and cirrhosis (e.g. cirrhosis of the liver).

Also, provided herein is a method of treating a cancer (e.g., any one ofcancers described herein), the method comprising the step ofadministering to a subject in need thereof a therapeutically effectiveamount of a pharmaceutical composition comprising the compositioncomprising a non-covalently bound complex comprising cabazitaxel andhuman serum albumin as described herein, and a pharmaceuticallyacceptable carrier.

In some embodiments, the cancer is selected from the group consisting ofbladder cancer, brain cancer, breast cancer, colorectal cancer, cervicalcancer, gastrointestinal cancer, genitourinary cancer, head and neckcancer, lung cancer, ovarian cancer, pancreatic cancer, prostate cancer,renal cancer, skin cancer, and testicular cancer.

In some embodiments, cancer is selected from sarcoma, angiosarcoma,fibrosarcoma, rhabdomyosarcoma, liposarcoma, myxoma, rhabdomyoma,fibroma, lipoma, teratoma, non-small cell lung cancer (NSCLC),bronchogenic carcinoma squamous cell, undifferentiated small cell,undifferentiated large cell, adenocarcinoma, alveolar bronchiolarcarcinoma, bronchial adenoma, sarcoma, lymphoma, chondromatoushamartoma, mesothelioma, gastrointestinal cancer, cancer of theesophagus, squamous cell carcinoma, adenocarcinoma, leiomyosarcoma,lymphoma, cancer of the stomach, carcinoma, lymphoma, leiomyosarcoma,cancer of the pancreas, ductal adenocarcinoma, insulinoma, glucagonoma,gastrinoma, carcinoid tumor, vipoma, cancer of the small bowel,adenocarcinoma, lymphoma, carcinoid tumors, Kaposi's sarcoma, leiomyoma,hemangioma, lipoma, neurofibroma, fibroma, cancer of the large bowel orcolon, tubular adenoma, villous adenoma, hamartoma, leiomyoma,genitourinary tract cancer, cancer of the kidney adenocarcinoma, Wilm'stumor (nephroblastoma), lymphoma, leukemia, cancer of the bladder,cancer of the urethra, squamous cell carcinoma, transitional cellcarcinoma, cancer of the prostate, cancer of the testis, seminoma,teratoma, embryonal carcinoma, teratocarcinoma, choriocarcinoma,sarcoma, interstitial cell carcinoma, fibroma, fibroadenoma, adenomatoidtumors, lipoma, liver cancer, hepatoma hepatocellular carcinoma,cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellularadenoma, hemangioma, bone cancer, osteogenic sarcoma (osteosarcoma),fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing'ssarcoma, malignant lymphoma (reticulum cell sarcoma), multiple myeloma,malignant giant cell tumor, chordoma, osteochrondroma(osteocartilaginous exostoses), benign chondroma, chondroblastoma,chondromyxofibroma, osteoid osteoma giant cell tumor, nervous systemcancer, cancer of the skull, osteoma, hemangioma, granuloma, xanthoma,osteitis deformans, cancer of the meninges meningioma, meningiosarcoma,gliomatosis, cancer of the brain, astrocytoma, medulloblastoma, glioma,ependymoma, germinoma (pinealoma), glioblastoma multiforme,oligodendroglioma, schwannoma, retinoblastoma, congenital tumors, cancerof the spinal cord, neurofibroma, meningioma, glioma, sarcoma,gynecological cancer, cancer of the uterus, endometrial carcinoma,cancer of the cervix, cervical carcinoma, pre tumor cervical dysplasia,cancer of the ovaries, ovarian carcinoma, serous cystadenocarcinoma,mucinous cystadenocarcinoma, unclassified carcinoma, granulosa-thecacell tumor, Sertoli Leydig cell tumor, dysgerminoma, malignant teratoma,cancer of the vulva, squamous cell carcinoma, intraepithelial carcinoma,adenocarcinoma, fibrosarcoma, melanoma, cancer of the vagina, clear cellcarcinoma, squamous cell carcinoma, botryoid sarcoma, embryonalrhabdomyosarcoma, cancer of the fallopian tubes, hematologic cancer,cancer of the blood, acute myeloid leukemia (AML), chronic myeloidleukemia (CML), acute lymphoblastic leukemia (ALL), chroniclymphoblastic leukemia, chronic lymphocytic leukemia, myeloproliferativediseases, multiple myeloma, myelodysplastic syndrome, Hodgkin'slymphoma, non-Hodgkin's lymphoma (malignant lymphoma), Waldenstrom'smacroglobulinemia, skin cancer, malignant melanoma, basal cellcarcinoma, squamous cell carcinoma, Kaposi's sarcoma, moles dysplasticnevi, lipoma, angioma, dermatofibroma, keloids, psoriasis, adrenal glandcancer, and neuroblastoma.

As used herein, an “effective amount,” “therapeutically effectiveamount,” or a “pharmaceutically-effective amount” in reference to thecompounds or compositions of the instant invention refers to the amountsufficient to induce a desired biological, pharmacological, ortherapeutic outcome in a subject. That result can be reduction,mitigation, delay, shortening the time to resolution of, alleviation ofthe signs or symptoms of, or exert a medically-beneficial effect uponthe underlying pathophysiology or pathogenesis of an expected orobserved side-effect, toxicity, disorder or condition, or any otherdesired alteration of a biological system. In cancer treatment, theresult will generally include the reduction, mitigation, limitation,and/or, delay of the deleterious physiological manifestations, growth ormetastases of neoplasms.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising a non-covalently bound complexcomprising cabazitaxel and human serum albumin as described herein,prednisone, and a pharmaceutically acceptable carrier.

In some embodiments, the method of treating cancer (e.g. any one ofcancers described herein) comprises the step of administering to asubject in need thereof of a therapeutically effective amount of acomposition comprising the composition comprising a non-covalently boundcomplex comprising cabazitaxel and human serum albumin as describedherein, and a therapeutically effective amount of at least one inhibitorof the following kinases for the treatment of cancer: PIM, Akt1, Akt2,Akt3, TGF-βR, PKA, PKG, PKC, CaM-kinase, phosphorylase kinase, MEKK,ERK, MAPK, mTOR, EGFR, HER2, HER3, HER4, INS-R, IGF-1R, IR-R, PDGFαR,PDGFβR, CSFIR, KIT, FLK-II, KDR/FLK-1, FLK-4, fit-1, FGFR1, FGFR2,FGFR3, FGFR4, c-Met, Ron, Sea, TRKA, TRKB, TRKC, FLT3, VEGFR/Flt2, Flt4,EphA1, EphA2, EphA3, EphB2, EphB4, Tie2, Src, Fyn, Lck, Fgr, Btk, Fak,SYK, FRK, JAK, ABL, ALK and B-Raf.

In some embodiments, the method of treating cancer (e.g. any one ofcancers described herein) comprises the step of administering to asubject in need thereof of a therapeutically effective amount of apharmaceutical composition comprising the composition comprising anon-covalently bound complex comprising cabazitaxel and human serumalbumin as described herein, and a therapeutically effective amount ofat least one anti-cancer drug. Examples of an anti-cancer drug includeaberaterone, aberaterone acetate, abarelix, aldesleukin, alemtuzumab,alitretinoin, allopurinol, altretamine, anastrozole, arsenic trioxide,asparaginase, azacitidine, bavituximab, bevacizumab, bexarotene,bleomycin, bortezombi, bortezomib, busulfan intravenous, busulfan oral,calusterone, capecitabine, carboplatin, carmustine, cetuximab,chlorambucil, cisplatin, cladribine, clofarabine, cyclophosphamide,cytarabine, dacarbazine, dactinomycin, dalteparin sodium, dasatinib,daunorubicin, decitabine, denileukin, denileukin diftitox, dexrazoxane,cabazitaxel, doxorubicin, dromostanolone propionate, eculizumab,enzalutamide, epirubicin, erlotinib, estramustine, etoposide phosphate,etoposide, exemestane, fentanyl citrate, filgrastim, floxuridine,fludarabine, fluorouracil, fulvestrant, gefitinib, gemcitabine,gemtuzumab ozogamicin, goserelin acetate, histrelin acetate, ibritumomabtiuxetan, idarubicin, ifosfamide, imatinib mesylate, interferon alfa 2a,irinotecan, lapatinib ditosylate, lenalidomide, letrozole, leucovorin,leuprolide acetate, levamisole, lomustine, meclorethamine, megestrolacetate, melphalan, mercaptopurine, methotrexate, methoxsalen, mitomycinC, mitotane, mitoxantrone, nandrolone phenpropionate, nelarabine,nofetumomab, oxaliplatin, paclitaxel, pamidronate, panitumumab,pegaspargase, pegfilgrastim, pemetrexed disodium, pentostatin,pipobroman, plicamycin, procarbazine, quinacrine, rasburicase,rituximab, ruxolitinib, sorafenib, streptozocin, sunitinib, sunitinibmaleate, tamoxifen, temozolomide, teniposide, testolactone, thalidomide,thioguanine, thiotepa, topotecan, toremifene, tositumomab, trastuzumab,tretinoin, uracil mustard, valrubicin, vinblastine, vincristine,vinorelbine, vorinostat and zoledronate.

In some embodiments, a composition comprising the composition comprisinga non-covalently bound complex comprising cabazitaxel and human serumalbumin as described herein and an anti-cancer drug are administeredsimultaneously.

In some embodiments, a composition comprising the composition comprisinga non-covalently bound complex comprising cabazitaxel and human serumalbumin as described herein and an anti-cancer drug are administeredconsecutively.

The composition comprising a non-covalently bound complex comprising thecabazitaxel and the human serum albumin described herein can beadministered to an individual, such as human, via various routes, suchas parenterally, including intravenous, intra-arterial, intraperitoneal,intrapulmonary, oral, inhalation, intravesicular, intramuscular,intra-tracheal, subcutaneous, intraocular, intrathecal, or transdermal.For example, the composition can be administered by inhalation to treatconditions of the respiratory tract. The composition can be used totreat respiratory conditions such as pulmonary fibrosis, broncheolitisobliterans, lung cancer, bronchoalveolar carcinoma, and the like. Insome embodiments, the composition described herein is administratedintravenously.

The methods described herein may be performed alone or in conjunctionwith another therapy, such as surgery, radiation, chemotherapy,immunotherapy, gene therapy, and the like. Additionally, a person havinga greater risk of developing the proliferative disease may receivetreatments to inhibit and/or delay the development of the disease.

As will be understood by those of ordinary skill in the art, theappropriate doses of cabazitaxel will be approximately those alreadyemployed in clinical therapies wherein cabazitaxel is administered aloneor in combination with other chemotherapeutic agents. Variation indosage will likely occur depending on the condition being treated.Appropriate effective doses will also vary, as recognized by thoseskilled in the art, depending on the severity of the disease, the routeof administration, the sex, age and general health condition of thesubject, excipient usage, the possibility of co-usage with othertherapeutic treatments such as use of other agents, and the judgment ofthe treating physician. For example, guidance for selecting an effectivedose can be determined by reference to the prescribing information forcabazitaxel.

Also, provided herein is a composition consisting essentially of humanserum albumin and non-covalently bound complexes of cabazitaxel andhuman serum albumin, wherein the cabazitaxel and the human serum albuminin the composition have a ratio by weight from about 1:10 to about1:3000.

Also, provided herein is a composition comprising a non-covalently boundcomplex consisting essentially of the cabazitaxel and the human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:10 to about 1:3000.

Also, provided herein is a composition comprising cabazitaxel and humanserum albumin, wherein the cabazitaxel and the human serum albumin inthe composition have a ratio by weight from about 1:10 to about 1:3000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, and wherein the composition has asolubility in an aqueous solution of at least 10 mg/mL. In someembodiments, the composition has a solubility in an aqueous solution ofabout 10 mg/mL, about 20 mg/mL, about 30 mg/mL, about 40 mg/mL, about 50mg/mL, 60 mg/mL, about 70 mg/mL, about 80 mg/mL, about 90 mg/mL, about100 mg/mL, about 150 mg/mL, or about 200 mg/mL. In some embodiments, thepH of the composition is neutral (e.g., pH of the composition is fromabout 5 to about 8, from about 5.5 to about 7.5, or from about 6 toabout 7, or the pH of the composition is about 5, about 5.5, about 6,about 6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about6.7, about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3,about 7.4, about 7.5, or about 8).

In some embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:50 to about 1:1500, fromabout 1:100 to about 1:800, from about 1:150 to about 1:600, or fromabout 1:200 to about 1:500. In some embodiments, the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:100 to about 1:2000. In some embodiments, the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000. In some embodiments, the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:800. In some embodiments, the cabazitaxel and the humanserum albumin in the composition have a ratio by weight from about 1:150to about 1:600. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:150 toabout 1:500. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:150 toabout 1:400. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:200 toabout 1:1000. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:200 toabout 1:800. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:200 toabout 1:600. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:200 toabout 1:500. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:200 toabout 1:400. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:250 toabout 1:1000. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:250 toabout 1:800. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:250 toabout 1:600. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:250 toabout 1:500. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:250 toabout 1:400. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:300 toabout 1:600. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:300 toabout 1:400. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:100 toabout 1:1000. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight from about 1:220 toabout 1:600. In some embodiments, the cabazitaxel and the human serumalbumin in the composition have a ratio by weight of about 1:200, 1:210,1:220, about 1:230, about 1:240, about 1:250, about 1:260, about 1:270,about 1:280, about 1:290, about 1:300, about 1:310, about 1:320, about1:330, about 1:340, about 1:350, about 1:360, about 1:370, about 1:380,about 1:390, about 1:400, about 1:450, about 1:460, about 1:500 or about1:600.

In some embodiments, the human serum albumin is a native human serumalbumin. In some embodiments, the human serum albumin is a recombinanthuman serum albumin. In some embodiments, the human serum albumin is afatty acid free human serum albumin. In some embodiments, the humanserum albumin is essentially fatty acid free. In some embodiments, thehuman serum albumin contains no more than two moles of fatty acids boundto one mole of human serum albumin. In some embodiments, the human serumalbumin contains no more than one mole of fatty acids bound to one moleof human serum albumin. In some embodiments, human serum albumincontains no more than 0.5 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.1 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.05 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.01 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.001 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0005 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0001 moles of fatty acids bound to one mole ofhuman serum albumin.

In some embodiments, the cabazitaxel can be a pharmaceuticallyacceptable salt of cabazitaxel. In some embodiments, the cabazitaxel canbe any one of crystal forms, amorphous forms, solvates and hydrates asdescribed herein.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 5 to about 8.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 6 to about 7.5.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 5 to about 8.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 6 to about 7.5.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 5 to about 8.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 6 to about 7.5.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in 0.9% saline. In some embodiments, the composition is aclear aqueous solution when the composition is dissolved in 5% dextrosesolution.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in an aqueous solvent, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solvent, when thecomposition is dissolved in an aqueous solution, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7.0, about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous solution is substantially free of solvent otherthan water. In some embodiments, the aqueous solution is free of solventother than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 5 to about 8, and wherein the clear aqueous solution issubstantially free of solvent other than water. In some embodiments,provided herein is a composition comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, wherein the composition has asolubility in an aqueous solution of at least 10 mg/mL, and wherein theclear aqueous solution has pH value from about 5 to about 8, and whereinthe clear aqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 6 to about 7.5, and wherein the clear aqueous solution issubstantially free of solvent other than water. In some embodiments,provided herein is a composition comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, wherein the composition has asolubility in an aqueous solution of at least 10 mg/mL, and wherein theclear aqueous solution has pH value from about 6 to about 7.5, andwherein the clear aqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 5 to about 8, and wherein the clear aqueous solution issubstantially free of solvent other than water. In some embodiments,provided herein is a composition comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, wherein the composition has asolubility in an aqueous solution of at least 10 mg/mL, and wherein theclear aqueous solution has pH value from about 5 to about 8, and whereinthe clear aqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent,wherein the composition has a solubility in an aqueous solution of atleast 10 mg/mL, and wherein the clear aqueous solution has pH value fromabout 6 to about 7.5, and wherein the clear aqueous solution issubstantially free of solvent other than water. In some embodiments,provided herein is a composition comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solvent, wherein the composition has asolubility in an aqueous solution of at least 10 mg/mL, and wherein theclear aqueous solution has pH value from about 6 to about 7.5, andwherein the clear aqueous solution is free of solvent other than water.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in water, wherein the clear aqueoussolution has pH value from about 5 to about 8. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 5.5 to about 7.8. In some embodiments, the composition forms aclear aqueous solution, when the composition is dissolved in water,wherein the clear aqueous solution has pH value from about 6 to about7.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in water, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in water, wherein the clear aqueous solutionhas pH value from about 6 to about 6.5. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 6.5 to about 7. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in water, whereinthe clear aqueous solution has pH value from about 7 to about 7.5. Insome embodiments, the composition forms a clear aqueous solution, whenthe composition is dissolved in water, wherein the clear aqueoussolution has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 0.9% saline, wherein the clearaqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 5.5 to about 7.8. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue from about 6 to about 7.5. In some embodiments, the compositionforms a clear aqueous solution, when the composition is dissolved in0.9% saline, wherein the clear aqueous solution has pH value from about6.5 to about 7.5. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in 0.9% saline,wherein the clear aqueous solution has pH value from about 6 to about6.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in 0.9% saline, wherein theclear aqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 7 to about 7.5. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 5% dextrose solution, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose olution, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7.0, about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 96% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 98% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99.5% of the total amountof cabazitaxel in the aqueous solution before the filtration. In someembodiments, the aqueous solution is free of solvent other than water.In some embodiments, the aqueous solution is substantially free ofsolvent other than water.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solution, wherein after theclear aqueous solution is filtered by a 0.22 micron filter, the amountof cabazitaxel in the filtered aqueous solution is at least 95%, 96%,97%, 98%, 99%, or 99.5% of the total amount of cabazitaxel in theaqueous solution before the filtration, wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 6 to about 7.5, and wherein the clear aqueoussolution is substantially free of solvent other than water. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 5 to about 8, and wherein the clear aqueous solutionis free of solvent other than water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in an aqueous solution, wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforethe filtration, wherein the clear aqueous solution has pH value fromabout 6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, the amount of cabazitaxel that is bound to the HSA(e.g., non-covalently) in the aqueous solution (e.g., clear aqueoussolution) comprising the composition comprising cabazitaxel and HSA (asdescribed herein) is at least 40%, at least 50%, at least 60%, at least70%, at least 80%, at least 90%, at least 95%, at least 99%, or about100% of the total about of cabazitaxel in the aqueous solution.

In some embodiments, the composition is an aqueous solution, whereinafter the aqueous solution is filtered by a 0.22 micron filter, theamount of cabazitaxel in the filtered aqueous solution is at least 80%of the total amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, the composition is an aqueous solution,wherein after the aqueous solution is filtered by a 0.22 micron filter,the amount of cabazitaxel in the filtered aqueous solution is at least85% of the total amount of cabazitaxel in the aqueous solution beforethe filtration. In some embodiments, the composition is an aqueoussolution, wherein after the aqueous solution is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 90% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, the aqueoussolution is free of solvent other than water. In some embodiments, theaqueous solution is substantially free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution for atleast 1 hour when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 2 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 3 hours when the composition isdissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 4 hours when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the composition is a clear aqueoussolution for at least 5 hours when the composition is dissolved in anaqueous solution (e.g. water, 0.9% saline, or 5% dextrose solution). Insome embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 8 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 24 hours when the compositionis dissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 3 days when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the aqueous solution is substantiallyfree of solvent other than water. In some embodiments, the aqueoussolution is free of solvent other than water.

In some embodiments, the composition is a solid formulation. Forexample, the solid formulation can be produced in a uniform manner bylyophilization. A skilled artisan would recognize other methods, such asrotary evaporation, that can also produce solid formulations.

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water. In some embodiments, the pH of the aqueousformulation (e.g., clear aqueous solution) is neutral (e.g., pH of thecomposition is from about 5 to about 8, from about 5.5 to about 7.5, orfrom about 6 to about 7, or the pH od the composition is about 5, about5.5, about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, about 7.5 or about 8).

In some embodiments, the aqueous formulation can be free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant selected from the group consisting of CREMOPHOR® surfactantsand Polysorbate 80.

In some embodiments, the aqueous formulation is a clear aqueoussolution. For example, the formulation can be a clear and stable aqueoussolution reconstituted from a sterile lyophilized powder. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation is substantially free of solvent otherthan water. In some embodiments, the aqueous formulation is a clearaqueous solution, wherein the aqueous formulation is free of solventother than water.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline. In some embodiments, theaqueous formulation is a clear aqueous solution reconstituted from thesolid formulation (e.g. the sterile lyophilized powder) in 5% dextrosesolution.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 5 to about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 5 to about 8.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 5 to about 8. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinthe pH of 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 5 to about 8. In some aspects of theaforementioned embodiments, the concentration of the reconstituted solidin the aqueous formulation is about 25 mg, about 50 mg, about 75 mg,about 100 mg, about 150 mg or 200 mg per 1 mL of the aqueous solvent. Insome aspects of the aforementioned embodiments, the concentration of thereconstituted solid in the aqueous formulation is from about 10 mg toabout 200 mg per 1 mL of the aqueous solvent.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 6 to about 7.5. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinpH of the 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value of about 6, about 6.1, about 6.2, about6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9,about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, orabout 8. In some embodiments, the aqueous formulation is a clear aqueoussolution reconstituted from the solid formulation (e.g. the sterilelyophilized powder) in 0.9% saline solution, wherein the pH of 0.9%saline solution is about 5.4, and wherein the aqueous formulation has pHvalue of about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, about 7.5, or about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose water solution, wherein pH of the 5% dextrose solution is about4.4, and wherein the aqueous formulation has pH value of about 6, about6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7,about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about7.4, about 7.5, or about 8.

In some embodiments, the aqueous formulation has pH value from about 5to about 8. In some embodiments, the aqueous formulation has pH valuefrom about 5.5 to about 7.8. In some embodiments, the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation has pH value from about 6.5 to about 7.5. Insome embodiments, the aqueous formulation has pH value from about 6 toabout 6.5. In some embodiments, the aqueous formulation has pH valuefrom about 6.5 to about 7. In some embodiments, the aqueous formulationhas pH value from about 7 to about 7.5. In some embodiments, the aqueousformulation has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water.

In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 5 toabout 8, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 5 to about 8, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 5.5 to about 7.8, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 5.5 to about7.8, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about7.5, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 6.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 6.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about 7,and wherein the aqueous formulation is free of solvent other than water.In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 7 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 7 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value about 6, about 6.1, about 6.2, about 6.3, about 6.4, about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1,about 7.2, about 7.3, about 7.4, or about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value about 6, about 6.1, about6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8,about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, orabout 7.5, and wherein the aqueous formulation is free of solvent otherthan water.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 95% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 96% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, after the aqueous formulation is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 98% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration. In some embodiments, after the aqueousformulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 99% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 99.5% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is substantially freeof solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is substantially free of solvent other thanwater. In some embodiments, after the aqueous formulation (e.g. a clearaqueous solution) is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before filtration, wherein the clear aqueous solution has pHvalue from about 5 to about 8, and wherein the clear aqueous solution isfree of solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is free of solvent other than water. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 80% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 85% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 90% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, the aqueous formulation is a clear aqueous solutionfor at least 1 hour. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 2 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 4 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 5 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 8 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 24 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours ata concentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is a clear aqueous solution for at least 24 hours. In someembodiments, the aqueous formulation is a transparent aqueous solutionfor at least 24 hours at a concentration of from about 5 mg/mL to about250 mg/mL, from about 10 mg/mL to about 200 mg/mL, from about 25 mg/mLto about 150 mg/mL, from about 10 mg/mL to about 50 mg/mL, from about 50mg/mL to about 100 mg/mL, from about 100 mg/mL to about 150 mg/mL, fromabout 150 mg/mL to about 200 mg/mL, or about 5 mg/mL, about 10 mg/mL,about 20 mg/mL, about 30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60mg/mL, about 70 mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100mg/mL at a temperature from about 1° C. to about 35° C., about 1° C. toabout 10° C., about 10° C. to about 20° C., about 20° C. to about 35°C., or about 1° C., about 5° C., about 10° C., about 15° C., about 20°C., about 25° C., about 30° C., or about 35° C. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 days. Insome embodiments, the aqueous formulation is a transparent aqueoussolution for at least 3 days when dissolved in an aqueous solution at aconcentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is free of solvent other thanwater.

Also, provided herein is a pharmaceutical composition comprising thecomposition comprising the cabazitaxel and the human serum albumin asdescribed herein, and a pharmaceutically acceptable carrier.

In some embodiments, the pharmaceutical composition is free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80.

In some embodiments, the pharmaceutical composition is substantiallyfree of a surfactant, such as CREMOPHOR® surfactants and Polysorbate 80.

Also, provided herein is a method of treating a proliferative diseasecomprising the step of administering to a subject in need thereof atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

Also, provided herein is a method of treating a cancer, the methodcomprising the step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

In some embodiments, the cancer is any one of cancers described herein.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, prednisone, and a pharmaceuticallyacceptable carrier.

In some embodiments, the method of treating cancer (e.g. any one ofcancers described herein) comprises the step of administering to asubject in need thereof a therapeutically effective amount of apharmaceutical composition comprising the composition comprising thecabazitaxel and the human serum albumin as described herein and atherapeutically effective amount of at least one inhibitor of thekinases for the treatment of cancer described herein.

In some embodiments, the method of treating cancer (e.g. any one ofcancers described herein) comprises the step of administering to asubject in need thereof a therapeutically effective amount of apharmaceutical composition comprising the composition comprising thecabazitaxel and the human serum albumin as described herein and atherapeutically effective amount of at least one anti-cancer drugdescribed herein.

In some embodiments, a composition comprising the cabazitaxel and thehuman serum albumin as described herein and an anti-cancer drug areadministered simultaneously.

In some embodiments, a composition comprising the cabazitaxel and thehuman serum albumin as described herein and an anti-cancer drug areadministered consecutively.

The compositions comprising the cabazitaxel and the human serum albumindescribed herein can be administered to an individual, such as human,via various routes, such as parenterally, including intravenous,intra-arterial, intraperitoneal, intrapulmonary, oral, inhalation,intravesicular, intramuscular, intra-tracheal, subcutaneous,intraocular, intrathecal, or transdermal. For example, the compositioncan be administered by inhalation to treat conditions of the respiratorytract. The composition can be used to treat respiratory conditions suchas pulmonary fibrosis, broncheolitis obliterans, lung cancer,bronchoalveolar carcinoma, and the like. In some embodiments, thenanoparticle composition is administrated intravenously.

The methods described herein may be performed alone or in conjunctionwith another therapy, such as surgery, radiation, chemotherapy,immunotherapy, gene therapy, and the like. Additionally, a person havinga greater risk of developing the proliferative disease may receivetreatments to inhibit or and/or delay the development of the disease.

As will be understood by those of ordinary skill in the art, theappropriate doses of cabazitaxel will be approximately those alreadyemployed in clinical therapies wherein cabazitaxel is administered aloneor in combination with other chemotherapeutic agents. Variation indosage will likely occur depending on the condition being treated.Appropriate effective doses will also vary, as recognized by thoseskilled in the art, depending on the severity of the disease, the routeof administration, the sex, age and general health condition of thesubject, excipient usage, the possibility of co-usage with othertherapeutic treatments such as use of other agents, and the judgment ofthe treating physician. For example, guidance for selecting an effectivedose can be determined by reference to the prescribing information forcabazitaxel.

Also, provided herein is a composition comprising cabazitaxel and humanserum albumin, wherein the cabazitaxel and the human serum albumin inthe composition have a ratio by weight from about 1:100 to about 1:3000.In some embodiments, the pH of the composition is neutral (e.g., pH ofthe composition is from about 5 to about 8, from about 5.5 to about 7.5,or from about 6 to about 7, or the pH of the composition is about 5,about 5.5, about 6, about 6.1, about 6.2, about 6.3, about 6.4, about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1,about 7.2, about 7.3, about 7.4, about 7.5, or about 8).

In some embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:2000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:220 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight of about 1:200, 1:210, 1:220, about1:230, about 1:240, about 1:250, about 1:260, about 1:270, about 1:280,about 1:290, about 1:300, about 1:310, about 1:320, about 1:330, about1:340, about 1:350, about 1:360, about 1:370, about 1:380, about 1:390,about 1:400, about 1:450, about 1:460, about 1:500 or about 1:600.

In some embodiments, the human serum albumin is a native human serumalbumin.

In some embodiments, the human serum albumin is a recombinant humanserum albumin. In some embodiments, the human serum albumin is a fattyacid free human serum albumin. In some embodiments, the human serumalbumin is essentially fatty acid free. In some embodiments, the humanserum albumin contains no more than two moles of fatty acids bound toone mole of human serum albumin. In some embodiments, the human serumalbumin contains no more than one mole of fatty acids bound to one moleof human serum albumin. In some embodiments, human serum albumincontains no more than 0.5 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.1 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.05 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.01 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.001 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0005 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0001 moles of fatty acids bound to one mole ofhuman serum albumin.

In some embodiments, the cabazitaxel can be a pharmaceuticallyacceptable salt of cabazitaxel. In some embodiments, cabazitaxel can beany one of crystal forms, amorphous forms, solvates and hydrates asdescribed herein.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent. In some embodiments,the aqueous solution is substantially free of solvent other than water.In some embodiments, the aqueous solution is free of solvent other thanwater.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in 0.9% saline. In some embodiments, the composition is aclear aqueous solution when the composition is dissolved in 5% dextrosesolution.

As used herein, the term “aqueous solution” refers to a solution,wherein at least one solvent is water and the weight % of water in themixture of solvents is at least 50%, at least 60%, at least 70% or atleast 90%. In some embodiments, aqueous solution is a solution in whichwater is the only solvent. In some embodiments, aqueous solution is 0.9%saline solution. In some embodiments, aqueous solution is 5% dextrosewater solution. In some embodiments, aqueous solution is a buffer (e.g.,phosphate buffer or a carbonate buffer). In some embodiments, the bufferis physiological buffer or a pharmaceutically acceptable buffer. In someembodiments, the buffer is any one of buffers described, for example, inY.-C. Lee et al. International Journal of Pharmaceutics 253 (2003)111-119, the disclosure of which is incorporated herein by reference inits entirety. In some embodiments, the buffer comprises maleic acid,tartaric acid, lactic acid, citric acid, acetic acid, sodiumbicarbonate, sodium phosphate, or mixtures thereof. In some embodiments,the pH range of the buffer is from about 3 to about 9, from about 4 toabout 8, from about 5 to about 7, from about 6 to about 7, from about 3to about 5, from about 3 to about 7, from about 4 to about 6, or fromabout 6 to about 6. In some embodiments, the pH of the buffer is about4, about 5, about 6, about 6.4, about 6.5, about 6.6, about 7, about7.5, or about 8.

As used herein, the term “aqueous solvent” refer to a liquid comprisingat least 50%, at least 60%, at least 70%, at least 90% or at least 95%water. In some embodiments, aqueous solvent is water.

As used herein, “substantially free of solvent,” in reference to anaqueous solution, refers to an aqueous solution that contains less than0.5%, by weight, of any non-water solvent. In some embodiments, theaqueous solution contains less than 0.1%, by weight, of any non-watersolvent. In some embodiments, the aqueous solution contains less than0.05%, by weight, of any non-water solvent.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 5 to about 8.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 6 to about7.5.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 5 to about 8.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 6 to about7.5.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 5 to about 8.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 6 to about7.5.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 5 to about 8,and wherein the clear aqueous solution is substantially free of solventother than water. In some embodiments, provided herein is a compositioncomprising cabazitaxel and human serum albumin, wherein the cabazitaxeland the human serum albumin in the composition have a ratio by weightfrom about 1:150 to about 1:1000, wherein the composition is a clearaqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8, and wherein the clear aqueous solution is free of solventother than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 5 to about 8,and wherein the clear aqueous solution is substantially free of solventother than water. In some embodiments, provided herein is a compositioncomprising cabazitaxel and human serum albumin, wherein the cabazitaxeland the human serum albumin in the composition have a ratio by weightfrom about 1:200 to about 1:600, wherein the composition is a clearaqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8, and wherein the clear aqueous solution is free of solventother than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 5 to about 8,and wherein the clear aqueous solution is substantially free of solventother than water. In some embodiments, provided herein is a compositioncomprising cabazitaxel and human serum albumin, wherein the cabazitaxeland the human serum albumin in the composition have a ratio by weightfrom about 1:250 to about 1:500, wherein the composition is a clearaqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8, and wherein the clear aqueous solution is free of solventother than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:150 to about 1:1000, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 6 to about7.5, and wherein the clear aqueous solution is substantially free ofsolvent other than water. In some embodiments, provided herein is acomposition comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:150 to about 1:1000, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:200 to about 1:600, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 6 to about7.5, and wherein the clear aqueous solution is substantially free ofsolvent other than water. In some embodiments, provided herein is acomposition comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:200 to about 1:600, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, provided herein is a composition comprisingcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:500, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solution, andwherein the clear aqueous solution has pH value from about 6 to about7.5, and wherein the clear aqueous solution is substantially free ofsolvent other than water. In some embodiments, provided herein is acomposition comprising cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:250 to about 1:500, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in an aqueous solvent, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent wherein the clear aqueoussolution has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous solution is substantially free of solvent otherthan water. In some embodiments, the aqueous solution is free of solventother than water.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in water, wherein the clear aqueoussolution has pH value from about 5 to about 8. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 5.5 to about 7.8. In some embodiments, the composition forms aclear aqueous solution, when the composition is dissolved in water,wherein the clear aqueous solution has pH value from about 6 to about7.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in water, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in water, wherein the clear aqueous solutionhas pH value from about 6 to about 6.5. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 6.5 to about 7. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in water, whereinthe clear aqueous solution has pH value from about 7 to about 7.5. Insome embodiments, the composition forms a clear aqueous solution, whenthe composition is dissolved in water, wherein the clear aqueoussolution has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 0.9% saline, wherein the clearaqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 5.5 to about 7.8. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue from about 6 to about 7.5. In some embodiments, the compositionforms a clear aqueous solution, when the composition is dissolved in0.9% saline, wherein the clear aqueous solution has pH value from about6.5 to about 7.5. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in 0.9% saline,wherein the clear aqueous solution has pH value from about 6 to about6.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in 0.9% saline, wherein theclear aqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 7 to about 7.5. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 5% dextrose solution, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose olution, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7.0, about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 96% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 98% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99.5% of the total amountof cabazitaxel in the aqueous solution before the filtration. In someembodiments, the aqueous solution is free of solvent other than water.In some embodiments, the aqueous solution is substantially free ofsolvent other than water.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solution, wherein after theclear aqueous solution is filtered by a 0.22 micron filter, the amountof cabazitaxel in the filtered aqueous solution is at least 95%, 96%,97%, 98%, 99%, or 99.5% of the total amount of cabazitaxel in theaqueous solution before the filtration, wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 6 to about 7.5, and wherein the clear aqueoussolution is substantially free of solvent other than water. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 5 to about 8, and wherein the clear aqueous solutionis free of solvent other than water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in an aqueous solution, wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforethe filtration, wherein the clear aqueous solution has pH value fromabout 6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, the amount of cabazitaxel that is bound to the HSA(e.g., non-covalently) in the aqueous solution (e.g., clear aqueoussolution) comprising the composition comprising cabazitaxel and HSA (asdescribed herein) is at least 40%, at least 50%, at least 60%, at least70%, at least 80%, at least 90%, at least 95%, at least 99%, or about100% of the total about of cabazitaxel in the aqueous solution.

In some embodiments, the composition is an aqueous solution, whereinafter the aqueous solution is filtered by a 0.22 micron filter, theamount of cabazitaxel in the filtered aqueous solution is at least 80%of the total amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, the composition is an aqueous solution,wherein after the aqueous solution is filtered by a 0.22 micron filter,the amount of cabazitaxel in the filtered aqueous solution is at least85% of the total amount of cabazitaxel in the aqueous solution beforethe filtration. In some embodiments, the composition is an aqueoussolution, wherein after the aqueous solution is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 90% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, the aqueoussolution is free of solvent other than water. In some embodiments, theaqueous solution is substantially free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution for atleast 1 hour when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 2 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 3 hours when the composition isdissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 4 hours when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the composition is a clear aqueoussolution for at least 5 hours when the composition is dissolved in anaqueous solution (e.g. water, 0.9% saline, or 5% dextrose solution). Insome embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 8 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 24 hours when the compositionis dissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 3 days when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the aqueous solution is substantiallyfree of solvent other than water. In some embodiments, the aqueoussolution is free of solvent other than water.

In some embodiments, the composition is a solid formulation. Forexample, the solid formulation can be produced in a uniform manner bylyophilization. A skilled artisan would recognize other methods, such asrotary evaporation, that can also produce solid formulations.

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water. In some embodiments, the aqueousformulation includes water and water-miscible organic solvents includingat least one of polyethylene glycol 300, polyethylene glycol 400,ethanol, methanol, propylene glycol, glycerin, N-methyl-2-pyrrolidone,dimethylacetamide, and dimethylsulfoxide. For example, thewater-miscible organic solvent can include ethanol. In some embodiments,the aqueous formulation includes water and ethanol. In some embodiments,the water-miscible organic solvent can be a mixture of water-miscibleorganic solvents. In some embodiments, the pH of the aqueous formulation(e.g., clear aqueous solution) is neutral (e.g., pH of the compositionis from about 5 to about 8, from about 5.5 to about 7.5, or from about 6to about 7, or the pH od the composition is about 5, about 5.5, about 6,about 6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about6.7, about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3,about 7.4, about 7.5 or about 8).

In some embodiments, the aqueous formulation can be free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant selected from the group consisting of CREMOPHOR® surfactantsand Polysorbate 80.

As used herein, the term “substantially free of surfactant” refers to aformulation containing less than 0.0005%, less than 0.0003%, or lessthan 0.0001% of surfactants and/or less than 0.0005%, less than 0.0003%,or less than 0.0001% of surfactant.

In some embodiments, the aqueous formulation is a clear aqueoussolution. For example, the formulation can be a clear and stable aqueoussolution reconstituted from a sterile lyophilized powder. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation is substantially free of solvent otherthan water. In some embodiments, the aqueous formulation is a clearaqueous solution, wherein the aqueous formulation is free of solventother than water.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline. In some embodiments, theaqueous formulation is a clear aqueous solution reconstituted from thesolid formulation (e.g. the sterile lyophilized powder) in 5% dextrosesolution.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 5 to about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 5 to about 8.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 5 to about 8. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinthe pH of 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 5 to about 8. In some aspects of theaforementioned embodiments, the concentration of the reconstituted solidin the aqueous formulation is about 25 mg, about 50 mg, about 75 mg,about 100 mg, about 150 mg or 200 mg per 1 mL of the aqueous solvent. Insome aspects of the aforementioned embodiments, the concentration of thereconstituted solid in the aqueous formulation is from about 10 mg toabout 200 mg per 1 mL of the aqueous solvent.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 6 to about 7.5. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinpH of the 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value of about 6, about 6.1, about 6.2, about6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9,about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, orabout 8. In some embodiments, the aqueous formulation is a clear aqueoussolution reconstituted from the solid formulation (e.g. the sterilelyophilized powder) in 0.9% saline solution, wherein the pH of 0.9%saline solution is about 5.4, and wherein the aqueous formulation has pHvalue of about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, about 7.5, or about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose water solution, wherein pH of the 5% dextrose solution is about4.4, and wherein the aqueous formulation has pH value of about 6, about6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7,about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about7.4, about 7.5, or about 8.

In some embodiments, the aqueous formulation has pH value from about 5to about 8. In some embodiments, the aqueous formulation has pH valuefrom about 5.5 to about 7.8. In some embodiments, the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation has pH value from about 6.5 to about 7.5. Insome embodiments, the aqueous formulation has pH value from about 6 toabout 6.5. In some embodiments, the aqueous formulation has pH valuefrom about 6.5 to about 7. In some embodiments, the aqueous formulationhas pH value from about 7 to about 7.5. In some embodiments, the aqueousformulation has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water.

In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 5 toabout 8, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 5 to about 8, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 5.5 to about 7.8, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 5.5 to about7.8, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about7.5, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 6.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 6.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about 7,and wherein the aqueous formulation is free of solvent other than water.In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 7 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 7 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value about 6, about 6.1, about 6.2, about 6.3, about 6.4, about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1,about 7.2, about 7.3, about 7.4, or about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value about 6, about 6.1, about6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8,about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, orabout 7.5, and wherein the aqueous formulation is free of solvent otherthan water.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 95% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 96% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, after the aqueous formulation is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 98% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration. In some embodiments, after the aqueousformulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 99% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 99.5% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is substantially freeof solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is substantially free of solvent other thanwater. In some embodiments, after the aqueous formulation (e.g. a clearaqueous solution) is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before filtration, wherein the clear aqueous solution has pHvalue from about 5 to about 8, and wherein the clear aqueous solution isfree of solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is free of solvent other than water. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 80% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 85% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 90% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, when the composition comprising cabazitaxel and HSAas described herein (e.g., sterile solid powder) is dissolved in anaqueous solvent (e.g., water, 0.9% saline or 5% dextrose), the resultantaqueous solution, when filtered using a 0.22 micron filter, comprises atleast 99% at the time of preparation, at least 99% after 1 hour, atleast 99% after 2 hours, at least 98% after 3 hours, at least 98% after4 hours, at least 98% after 5 hours, at least 98% after 6 hours, or atleast 98% after 24 hours of the amount of cabazitaxel used to preparethe composition.

In some embodiments, when the composition comprising cabazitaxel and HSAas described herein (e.g., sterile solid powder) is dissolved in anaqueous solvent (e.g., water, 0.9% saline or 5% dextrose), the resultantaqueous solution, when filtered using a 0.22 micron filter, comprises atleast 99% at the time of preparation, at least 99% after 1 hour, atleast 99% after 2 hours, at least 99% after 3 hours, at least 99% after4 hours, at least 99% after 5 hours, at least 99% after 6 hours, or atleast 99% after 24 hours of the amount of cabazitaxel used to preparethe composition.

In some embodiments, when the composition comprising cabazitaxel and HSAas described herein (e.g., sterile solid powder) is dissolved in anaqueous solvent (e.g., water, 0.9% saline or 5% dextrose), the resultantaqueous solution, when filtered using a 0.22 micron filter, comprises atleast 98% at the time of preparation, at least 98% after 1 hour, atleast 98% after 2 hours, at least 98% after 3 hours, at least 98% after4 hours, at least 98% after 5 hours, at least 98% after 6 hours, or atleast 98% after 24 hours of the amount of cabazitaxel used to preparethe composition.

In some embodiments, when the composition comprising cabazitaxel and HSAas described herein (e.g., sterile solid powder) is dissolved in anaqueous solvent (e.g., water, 0.9% saline or 5% dextrose), the resultantaqueous solution, when filtered using a 0.22 micron filter, comprises atleast 97% at the time of preparation, at least 97% after 1 hour, atleast 97% after 2 hours, at least 97% after 3 hours, at least 97% after4 hours, at least 97% after 5 hours, at least 97% after 6 hours, or atleast 97% after 24 hours of the amount of cabazitaxel used to preparethe composition.

In some embodiments, when the composition comprising cabazitaxel and HSAas described herein (e.g., sterile solid powder) is dissolved in anaqueous solvent (e.g., water, 0.9% saline or 5% dextrose), the resultantaqueous solution, when filtered using a 0.22 micron filter, comprises atleast 96% at the time of preparation, at least 96% after 1 hour, atleast 96% after 2 hours, at least 96% after 3 hours, at least 96% after4 hours, at least 96% after 5 hours, at least 96% after 6 hours, or atleast 96% after 24 hours of the amount of cabazitaxel used to preparethe composition.

In some embodiments, when the composition comprising cabazitaxel and HSAas described herein (e.g., sterile solid powder) is dissolved in anaqueous solvent (e.g., water, 0.9% saline or 5% dextrose), the resultantaqueous solution, when filtered using a 0.22 micron filter, comprises atleast 95% at the time of preparation, at least 95% after 1 hour, atleast 95% after 2 hours, at least 95% after 3 hours, at least 95% after4 hours, at least 95% after 5 hours, at least 95% after 6 hours, or atleast 95% after 24 hours of the amount of cabazitaxel used to preparethe composition.

In some embodiments, the aqueous formulation is a clear aqueous solutionfor at least 1 hour. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 2 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 4 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 5 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 8 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 24 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours ata concentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is a clear aqueous solution for at least 24 hours. In someembodiments, the aqueous formulation is a transparent aqueous solutionfor at least 24 hours at a concentration of from about 5 mg/mL to about250 mg/mL, from about 10 mg/mL to about 200 mg/mL, from about 25 mg/mLto about 150 mg/mL, from about 10 mg/mL to about 50 mg/mL, from about 50mg/mL to about 100 mg/mL, from about 100 mg/mL to about 150 mg/mL, fromabout 150 mg/mL to about 200 mg/mL, or about 5 mg/mL, about 10 mg/mL,about 20 mg/mL, about 30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60mg/mL, about 70 mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100mg/mL at a temperature from about 1° C. to about 35° C., about 1° C. toabout 10° C., about 10° C. to about 20° C., about 20° C. to about 35°C., or about 1° C., about 5° C., about 10° C., about 15° C., about 20°C., about 25° C., about 30° C., or about 35° C. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 days. Insome embodiments, the aqueous formulation is a transparent aqueoussolution for at least 3 days when dissolved in an aqueous solution at aconcentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is free of solvent other thanwater.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 95% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 96% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, after the aqueous formulation is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 98% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration. In some embodiments, after the aqueousformulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 99% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 99.5% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is substantially freeof solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is substantially free of solvent other thanwater. In some embodiments, after the aqueous formulation (e.g. a clearaqueous solution) is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before filtration, wherein the clear aqueous solution has pHvalue from about 5 to about 8, and wherein the clear aqueous solution isfree of solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is free of solvent other than water. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 80% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 85% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 90% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

Also, provided herein is a pharmaceutical composition comprising thecomposition comprising the cabazitaxel and the human serum albumin asdescribed herein, and a pharmaceutically acceptable carrier.

In some embodiments, the pharmaceutical composition further comprises atleast one anti-cancer drug (e.g., any one of the anti-cancer drugs asdescribed herein).

In some embodiments, the pharmaceutical composition is free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the pharmaceutical composition is substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the pharmaceutical composition can be substantially free ofa surfactant selected from the group consisting of CREMOPHOR®surfactants and Polysorbate 80.

Also, provided herein is a method of treating a proliferative diseasecomprising the step of administering to a subject in need thereof apharmaceutical composition comprising the composition comprising thecabazitaxel and the human serum albumin as described herein, and apharmaceutically acceptable carrier.

Also, provided herein is a method of treating a cancer (e.g., any one ofcancers described herein), the method comprising the step ofadministering to a subject in need thereof of a therapeuticallyeffective amount of a pharmaceutical composition comprising thecomposition comprising the cabazitaxel and the human serum albumin asdescribed herein, and a pharmaceutically acceptable carrier.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition comprising the cabazitaxel and the humanserum albumin as described herein, prednisone, and a pharmaceuticallyacceptable carrier.

In some embodiments, the method of treating cancer (e.g., any one ofcancers described herein) comprises the step of administering to asubject in need thereof a therapeutically effective amount of apharmaceutical composition comprising the composition comprising thecabazitaxel and the human serum albumin as described herein, and atherapeutically effective amount of at least one inhibitor of thekinases for the treatment of cancer described herein.

In some embodiments, the method of treating cancer (e.g. any one ofcancers described herein) comprises the step of administering to asubject in need thereof a therapeutically effective amount of apharmaceutical composition comprising the composition comprising thecabazitaxel and the human serum albumin as described herein, and atherapeutically effective amount of at least one anti-cancer drugdescribed herein.

In some embodiments, a composition comprising the cabazitaxel and thehuman serum albumin as described herein and an anti-cancer drug areadministered simultaneously.

In some embodiments, a composition comprising the cabazitaxel and thehuman serum albumin as described herein and an anti-cancer drug areadministered consecutively.

The compositions comprising the cabazitaxel and the human serum albumindescribed herein can be administered to an individual, such as human,via various routes, such as parenterally, including intravenous,intra-arterial, intraperitoneal, intrapulmonary, oral, inhalation,intravesicular, intramuscular, intra-tracheal, subcutaneous,intraocular, intrathecal, or transdermal. For example, the compositioncan be administered by inhalation to treat conditions of the respiratorytract. The composition can be used to treat respiratory conditions suchas pulmonary fibrosis, broncheolitis obliterans, lung cancer,bronchoalveolar carcinoma, and the like. In some embodiments, thecomposition is administrated intravenously.

The methods described herein may be performed alone or in conjunctionwith another therapy, such as surgery, radiation, chemotherapy,immunotherapy, gene therapy, and the like. Additionally, a person havinga greater risk of developing the proliferative disease may receivetreatments to inhibit and/or delay the development of the disease.

As will be understood by those of ordinary skill in the art, theappropriate doses of cabazitaxel will be approximately those alreadyemployed in clinical therapies wherein cabazitaxel is administered aloneor in combination with other chemotherapeutic agents. Variation indosage will likely occur depending on the condition being treated.Appropriate effective doses will also vary, as recognized by thoseskilled in the art, depending on the severity of the disease, the routeof administration, the sex, age and general health condition of thesubject, excipient usage, the possibility of co-usage with othertherapeutic treatments such as use of other agents, and the judgment ofthe treating physician. For example, guidance for selecting an effectivedose can be determined by reference to the prescribing information forcabazitaxel.

Also, provided herein is a composition consisting essentially ofcabazitaxel and human serum albumin, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:10 to about 1:3000. In some embodiments, the pH of the composition isneutral (e.g., pH of the composition is from about 5 to about 8, fromabout 5.5 to about 7.5, or from about 6 to about 7, or the pH of thecomposition is about 5, about 5.5, about 6, about 6.1, about 6.2, about6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9,about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, orabout 8).

In some embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:2000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:220 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight of about 1:200, 1:210, 1:220, about1:230, about 1:240, about 1:250, about 1:260, about 1:270, about 1:280,about 1:290, about 1:300, about 1:310, about 1:320, about 1:330, about1:340, about 1:350, about 1:360, about 1:370, about 1:380, about 1:390,about 1:400, about 1:450, about 1:460, about 1:500 or about 1:600.

In some embodiments, the human serum albumin is a native human serumalbumin.

In some embodiments, the human serum albumin is a recombinant humanserum albumin. In some embodiments, the human serum albumin is a fattyacid free human serum albumin. In some embodiments, the human serumalbumin is essentially fatty acid free. In some embodiments, the humanserum albumin contains no more than two moles of fatty acids bound toone mole of human serum albumin. In some embodiments, the human serumalbumin contains no more than one mole of fatty acids bound to one moleof human serum albumin. In some embodiments, human serum albumincontains no more than 0.5 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.1 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.05 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.01 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.001 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0005 moles of fatty acids bound to one mole ofhuman serum albumin. In some embodiments, the human serum albumincontains no more than 0.0001 moles of fatty acids bound to one mole ofhuman serum albumin.

In some embodiments, the cabazitaxel can be a pharmaceuticallyacceptable salt of cabazitaxel. In some embodiments, cabazitaxel can beany one of crystal forms, amorphous forms, solvates and hydrates asdescribed herein.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent. In some embodiments,the aqueous solution is substantially free of solvent other than water.In some embodiments, the aqueous solution is free of solvent other thanwater.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in 0.9% saline. In some embodiments, the composition is aclear aqueous solution when the composition is dissolved in 5% dextrosesolution.

As used herein, the term “aqueous solution” refers to a solution,wherein at least one solvent is water and the weight % of water in themixture of solvents is at least 50%, at least 60%, at least 70% or atleast 90%. In some embodiments, aqueous solution is a solution in whichwater is the only solvent. In some embodiments, aqueous solution is 0.9%saline solution. In some embodiments, aqueous solution is 5% dextrosewater solution. In some embodiments, aqueous solution is a buffer (e.g.,phosphate buffer or a carbonate buffer). In some embodiments, the bufferis physiological buffer or a pharmaceutically acceptable buffer. In someembodiments, the buffer is any one of buffers described, for example, inY.-C. Lee et al. International Journal of Pharmaceutics 253 (2003)111-119, the disclosure of which is incorporated herein by reference inits entirety. In some embodiments, the buffer comprises maleic acid,tartaric acid, lactic acid, citric acid, acetic acid, sodiumbicarbonate, sodium phosphate, or mixtures thereof. In some embodiments,the pH range of the buffer is from about 3 to about 9, from about 4 toabout 8, from about 5 to about 7, from about 6 to about 7, from about 3to about 5, from about 3 to about 7, from about 4 to about 6, or fromabout 6 to about 6. In some embodiments, the pH of the buffer is about4, about 5, about 6, about 6.4, about 6.5, about 6.6, about 7, about7.5, or about 8.

As used herein, the term “aqueous solvent” refer to a liquid comprisingat least 50%, at least 60%, at least 70%, at least 90% or at least 95%water. In some embodiments, aqueous solvent is water.

As used herein, “substantially free of solvent,” in reference to anaqueous solution, refers to an aqueous solution that contains less than0.5%, by weight, of any non-water solvent. In some embodiments, theaqueous solution contains less than 0.1%, by weight, of any non-watersolvent. In some embodiments, the aqueous solution contains less than0.05%, by weight, of any non-water solvent.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:150 to about 1:1000, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:150 to about 1:1000, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:200 to about 1:600, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:200 to about 1:600, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:250 to about 1:500, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:250 to about 1:500, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:150 to about 1:1000, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8, and wherein the clear aqueous solution is substantiallyfree of solvent other than water. In some embodiments, provided hereinis a composition consisting essentially of cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solution, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:200 to about 1:600, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8, and wherein the clear aqueous solution is substantiallyfree of solvent other than water. In some embodiments, provided hereinis a composition consisting essentially of cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solution, and wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:250 to about 1:500, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about5 to about 8, and wherein the clear aqueous solution is substantiallyfree of solvent other than water. In some embodiments, provided hereinis a composition comprising cabazitaxel and human serum albumin, whereinthe cabazitaxel and the human serum albumin in the composition have aratio by weight from about 1:250 to about 1:500, wherein the compositionis a clear aqueous solution when the composition is dissolved in anaqueous solution, and wherein the clear aqueous solution has pH valuefrom about 5 to about 8, and wherein the clear aqueous solution is freeof solvent other than water.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:150 to about 1:1000, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5, and wherein the clear aqueous solution is substantiallyfree of solvent other than water. In some embodiments, provided hereinis a composition consisting essentially of cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solution, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:200 to about 1:600, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5, and wherein the clear aqueous solution is substantiallyfree of solvent other than water. In some embodiments, provided hereinis a composition consisting essentially of cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solution, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, provided herein is a composition consistingessentially of cabazitaxel and human serum albumin, wherein thecabazitaxel and the human serum albumin in the composition have a ratioby weight from about 1:250 to about 1:500, wherein the composition is aclear aqueous solution when the composition is dissolved in an aqueoussolution, and wherein the clear aqueous solution has pH value from about6 to about 7.5, and wherein the clear aqueous solution is substantiallyfree of solvent other than water. In some embodiments, provided hereinis a composition consisting essentially of cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500,wherein the composition is a clear aqueous solution when the compositionis dissolved in an aqueous solution, and wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is free of solvent other than water.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in an aqueous solvent, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in an aqueous solvent wherein the clear aqueoussolution has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous solution is substantially free of solvent otherthan water. In some embodiments, the aqueous solution is free of solventother than water.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in water, wherein the clear aqueoussolution has pH value from about 5 to about 8. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 5.5 to about 7.8. In some embodiments, the composition forms aclear aqueous solution, when the composition is dissolved in water,wherein the clear aqueous solution has pH value from about 6 to about7.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in water, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in water, wherein the clear aqueous solutionhas pH value from about 6 to about 6.5. In some embodiments, thecomposition forms a clear aqueous solution, when the composition isdissolved in water, wherein the clear aqueous solution has pH value fromabout 6.5 to about 7. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in water, whereinthe clear aqueous solution has pH value from about 7 to about 7.5. Insome embodiments, the composition forms a clear aqueous solution, whenthe composition is dissolved in water, wherein the clear aqueoussolution has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 0.9% saline, wherein the clearaqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 5.5 to about 7.8. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue from about 6 to about 7.5. In some embodiments, the compositionforms a clear aqueous solution, when the composition is dissolved in0.9% saline, wherein the clear aqueous solution has pH value from about6.5 to about 7.5. In some embodiments, the composition forms a clearaqueous solution, when the composition is dissolved in 0.9% saline,wherein the clear aqueous solution has pH value from about 6 to about6.5. In some embodiments, the composition forms a clear aqueoussolution, when the composition is dissolved in 0.9% saline, wherein theclear aqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 0.9% saline, wherein the clear aqueoussolution has pH value from about 7 to about 7.5. In some embodiments,the composition forms a clear aqueous solution, when the composition isdissolved in 0.9% saline, wherein the clear aqueous solution has pHvalue about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition forms a clear aqueous solution,when the composition is dissolved in 5% dextrose solution, wherein theclear aqueous solution has pH value from about 5 to about 8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 5.5 to about 7.8. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6 to about 6.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 6.5 to about 7. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value from about 7 to about 7.5. In someembodiments, the composition forms a clear aqueous solution, when thecomposition is dissolved in 5% dextrose solution, wherein the clearaqueous solution has pH value about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7.0, about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solvent (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 96% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solvent (e.g. water, 0.9% saline,or 5% dextrose solution), wherein after the clear aqueous solution isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 98% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution), wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 99.5% of the total amountof cabazitaxel in the aqueous solution before the filtration. In someembodiments, the aqueous solution is free of solvent other than water.In some embodiments, the aqueous solution is substantially free ofsolvent other than water.

In some embodiments, the composition is a clear aqueous solution whenthe composition is dissolved in an aqueous solution, wherein after theclear aqueous solution is filtered by a 0.22 micron filter, the amountof cabazitaxel in the filtered aqueous solution is at least 95%, 96%,97%, 98%, 99%, or 99.5% of the total amount of cabazitaxel in theaqueous solution before the filtration, wherein the clear aqueoussolution has pH value from about 5 to about 8, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 6 to about 7.5, and wherein the clear aqueoussolution is substantially free of solvent other than water. In someembodiments, the composition is a clear aqueous solution when thecomposition is dissolved in an aqueous solution, wherein after the clearaqueous solution is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before the filtration, wherein the clear aqueous solution haspH value from about 5 to about 8, and wherein the clear aqueous solutionis free of solvent other than water. In some embodiments, thecomposition is a clear aqueous solution when the composition isdissolved in an aqueous solution, wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforethe filtration, wherein the clear aqueous solution has pH value fromabout 6 to about 7.5, and wherein the clear aqueous solution is free ofsolvent other than water.

In some embodiments, the amount of cabazitaxel that is bound to the HSA(e.g., non-covalently) in the aqueous solution (e.g., clear aqueoussolution) comprising the composition consisting essentially ofcabazitaxel and HSA (as described herein) is at least 40%, at least 50%,at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, atleast 99%, or about 100% of the total about of cabazitaxel in theaqueous solution.

In some embodiments, the composition is an aqueous solution, whereinafter the aqueous solution is filtered by a 0.22 micron filter, theamount of cabazitaxel in the filtered aqueous solution is at least 80%of the total amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, the composition is an aqueous solution,wherein after the aqueous solution is filtered by a 0.22 micron filter,the amount of cabazitaxel in the filtered aqueous solution is at least85% of the total amount of cabazitaxel in the aqueous solution beforethe filtration. In some embodiments, the composition is an aqueoussolution, wherein after the aqueous solution is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 90% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, the aqueoussolution is free of solvent other than water. In some embodiments, theaqueous solution is substantially free of solvent other than water.

In some embodiments, the composition is a clear aqueous solution for atleast 1 hour when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 2 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 3 hours when the composition isdissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 4 hours when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the composition is a clear aqueoussolution for at least 5 hours when the composition is dissolved in anaqueous solution (e.g. water, 0.9% saline, or 5% dextrose solution). Insome embodiments, the composition is a clear aqueous solution for atleast 6 hours when the composition is dissolved in an aqueous solution(e.g. water, 0.9% saline, or 5% dextrose solution). In some embodiments,the composition is a clear aqueous solution for at least 8 hours whenthe composition is dissolved in an aqueous solution (e.g. water, 0.9%saline, or 5% dextrose solution). In some embodiments, the compositionis a clear aqueous solution for at least 24 hours when the compositionis dissolved in an aqueous solution (e.g. water, 0.9% saline, or 5%dextrose solution). In some embodiments, the composition is a clearaqueous solution for at least 3 days when the composition is dissolvedin an aqueous solution (e.g. water, 0.9% saline, or 5% dextrosesolution). In some embodiments, the aqueous solution is substantiallyfree of solvent other than water. In some embodiments, the aqueoussolution is free of solvent other than water.

In some embodiments, the composition is a solid formulation. Forexample, the solid formulation can be produced in a uniform manner bylyophilization. A skilled artisan would recognize other methods, such asrotary evaporation, that can also produce solid formulations.

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water. In some embodiments, the aqueousformulation includes water and water-miscible organic solvents includingat least one of polyethylene glycol 300, polyethylene glycol 400,ethanol, methanol, propylene glycol, glycerin, N-methyl-2-pyrrolidone,dimethylacetamide, and dimethylsulfoxide. For example, thewater-miscible organic solvent can include ethanol. In some embodiments,the aqueous formulation includes water and ethanol. In some embodiments,the water-miscible organic solvent can be a mixture of water-miscibleorganic solvents. In some embodiments, the pH of the aqueous formulation(e.g., clear aqueous solution) is neutral (e.g., pH of the compositionis from about 5 to about 8, from about 5.5 to about 7.5, or from about 6to about 7, or the pH od the composition is about 5, about 5.5, about 6,about 6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about6.7, about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3,about 7.4, about 7.5 or about 8).

In some embodiments, the aqueous formulation can be free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the aqueous formulation can be substantially free of asurfactant selected from the group consisting of CREMOPHOR® surfactantsand Polysorbate 80.

As used herein, the term “substantially free of surfactant” refers to aformulation containing less than 0.0005%, less than 0.0003%, or lessthan 0.0001% of surfactants and/or less than 0.0005%, less than 0.0003%,or less than 0.0001% of surfactant.

In some embodiments, the aqueous formulation is a clear aqueoussolution. For example, the formulation can be a clear and stable aqueoussolution reconstituted from a sterile lyophilized powder. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation is substantially free of solvent otherthan water. In some embodiments, the aqueous formulation is a clearaqueous solution, wherein the aqueous formulation is free of solventother than water.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline. In some embodiments, theaqueous formulation is a clear aqueous solution reconstituted from thesolid formulation (e.g. the sterile lyophilized powder) in 5% dextrosesolution.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 5 to about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 5 to about 8.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 5 to about 8. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 5 to about 8. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinthe pH of 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 5 to about 8. In some aspects of theaforementioned embodiments, the concentration of the reconstituted solidin the aqueous formulation is about 25 mg, about 50 mg, about 75 mg,about 100 mg, about 150 mg or 200 mg per 1 mL of the aqueous solvent.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 0.9% saline, wherein the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose solution, wherein the aqueous formulation has pH value fromabout 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value from about 6 to about 7.5. In someembodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in 0.9% saline solution, wherein the pH of 0.9% saline solutionis about 5.4, and wherein the aqueous formulation has pH value fromabout 6 to about 7.5. In some embodiments, the aqueous formulation is aclear aqueous solution reconstituted from the solid formulation (e.g.the sterile lyophilized powder) in 5% dextrose water solution, whereinpH of the 5% dextrose solution is about 4.4, and wherein the aqueousformulation has pH value from about 6 to about 7.5.

In some embodiments, the aqueous formulation is a clear aqueous solutionreconstituted from the solid formulation (e.g. the sterile lyophilizedpowder) in water, wherein the pH of water is about 7, and wherein theaqueous formulation has pH value of about 6, about 6.1, about 6.2, about6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9,about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, about 7.5, orabout 8. In some embodiments, the aqueous formulation is a clear aqueoussolution reconstituted from the solid formulation (e.g. the sterilelyophilized powder) in 0.9% saline solution, wherein the pH of 0.9%saline solution is about 5.4, and wherein the aqueous formulation has pHvalue of about 6, about 6.1, about 6.2, about 6.3, about 6.4, about 6.5,about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1, about7.2, about 7.3, about 7.4, about 7.5, or about 8. In some embodiments,the aqueous formulation is a clear aqueous solution reconstituted fromthe solid formulation (e.g. the sterile lyophilized powder) in 5%dextrose water solution, wherein pH of the 5% dextrose solution is about4.4, and wherein the aqueous formulation has pH value of about 6, about6.1, about 6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7,about 6.8, about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about7.4, about 7.5, or about 8.

In some embodiments, the aqueous formulation has pH value from about 5to about 8. In some embodiments, the aqueous formulation has pH valuefrom about 5.5 to about 7.8. In some embodiments, the aqueousformulation has pH value from about 6 to about 7.5. In some embodiments,the aqueous formulation has pH value from about 6.5 to about 7.5. Insome embodiments, the aqueous formulation has pH value from about 6 toabout 6.5. In some embodiments, the aqueous formulation has pH valuefrom about 6.5 to about 7. In some embodiments, the aqueous formulationhas pH value from about 7 to about 7.5. In some embodiments, the aqueousformulation has pH value about 6, about 6.1, about 6.2, about 6.3, about6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0,about 7.1, about 7.2, about 7.3, about 7.4, or about 7.5. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof solvent other than water.

In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 5 toabout 8, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 5 to about 8, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 5.5 to about 7.8, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 5.5 to about7.8, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about7.5, and wherein the aqueous formulation is free of solvent other thanwater. In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 6 toabout 6.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 6 to about 6.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value from about 6.5 to about 7, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value from about 6.5 to about 7,and wherein the aqueous formulation is free of solvent other than water.In some embodiments, the aqueous formulation is a clear aqueoussolution, wherein the aqueous formulation has pH value from about 7 toabout 7.5, and wherein the aqueous formulation is substantially free ofsolvent other than water. In some embodiments, the aqueous formulationis a clear aqueous solution, wherein the aqueous formulation has pHvalue from about 7 to about 7.5, and wherein the aqueous formulation isfree of solvent other than water. In some embodiments, the aqueousformulation is a clear aqueous solution, wherein the aqueous formulationhas pH value about 6, about 6.1, about 6.2, about 6.3, about 6.4, about6.5, about 6.6, about 6.7, about 6.8, about 6.9, about 7.0, about 7.1,about 7.2, about 7.3, about 7.4, or about 7.5, and wherein the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is a clear aqueous solution,wherein the aqueous formulation has pH value about 6, about 6.1, about6.2, about 6.3, about 6.4, about 6.5, about 6.6, about 6.7, about 6.8,about 6.9, about 7.0, about 7.1, about 7.2, about 7.3, about 7.4, orabout 7.5, and wherein the aqueous formulation is free of solvent otherthan water.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 95% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 96% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 97% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, after the aqueous formulation is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 98% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration. In some embodiments, after the aqueousformulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 99% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 99.5% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 95%, 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is substantially freeof solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is substantially free of solvent other thanwater. In some embodiments, after the aqueous formulation (e.g. a clearaqueous solution) is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 95%, 96%, 97%,98%, 99%, or 99.5% of the total amount of cabazitaxel in the aqueoussolution before filtration, wherein the clear aqueous solution has pHvalue from about 5 to about 8, and wherein the clear aqueous solution isfree of solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 95%, 96%, 97%, 98%, 99%, or 99.5% of the total amount ofcabazitaxel in the aqueous solution before filtration, wherein the clearaqueous solution has pH value from about 6 to about 7.5, and wherein theclear aqueous solution is free of solvent other than water. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 80% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 85% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 90% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

In some embodiments, when the composition consisting essentially ofcabazitaxel and HSA as described herein (e.g., sterile solid powder) isdissolved in an aqueous solvent (e.g., water, 0.9% saline or 5%dextrose), the resultant aqueous solution, when filtered using a 0.22micron filter, comprises at least 99% at the time of preparation, atleast 99% after 1 hour, at least 99% after 2 hours, at least 98% after 3hours, at least 98% after 4 hours, at least 98% after 5 hours, at least98% after 6 hours, or at least 98% after 24 hours of the amount ofcabazitaxel used to prepare the composition.

In some embodiments, when the composition consisting essentially ofcabazitaxel and HSA as described herein (e.g., sterile solid powder) isdissolved in an aqueous solvent (e.g., water, 0.9% saline or 5%dextrose), the resultant aqueous solution, when filtered using a 0.22micron filter, comprises at least 99% at the time of preparation, atleast 99% after 1 hour, at least 99% after 2 hours, at least 99% after 3hours, at least 99% after 4 hours, at least 99% after 5 hours, at least99% after 6 hours, or at least 99% after 24 hours of the amount ofcabazitaxel used to prepare the composition.

In some embodiments, when the composition consisting essentially ofcabazitaxel and HSA as described herein (e.g., sterile solid powder) isdissolved in an aqueous solvent (e.g., water, 0.9% saline or 5%dextrose), the resultant aqueous solution, when filtered using a 0.22micron filter, comprises at least 98% at the time of preparation, atleast 98% after 1 hour, at least 98% after 2 hours, at least 98% after 3hours, at least 98% after 4 hours, at least 98% after 5 hours, at least98% after 6 hours, or at least 98% after 24 hours of the amount ofcabazitaxel used to prepare the composition.

In some embodiments, when the composition consisting essentially ofcabazitaxel and HSA as described herein (e.g., sterile solid powder) isdissolved in an aqueous solvent (e.g., water, 0.9% saline or 5%dextrose), the resultant aqueous solution, when filtered using a 0.22micron filter, comprises at least 97% at the time of preparation, atleast 97% after 1 hour, at least 97% after 2 hours, at least 97% after 3hours, at least 97% after 4 hours, at least 97% after 5 hours, at least97% after 6 hours, or at least 97% after 24 hours of the amount ofcabazitaxel used to prepare the composition.

In some embodiments, when the composition consisting essentially ofcabazitaxel and HSA as described herein (e.g., sterile solid powder) isdissolved in an aqueous solvent (e.g., water, 0.9% saline or 5%dextrose), the resultant aqueous solution, when filtered using a 0.22micron filter, comprises at least 96% at the time of preparation, atleast 96% after 1 hour, at least 96% after 2 hours, at least 96% after 3hours, at least 96% after 4 hours, at least 96% after 5 hours, at least96% after 6 hours, or at least 96% after 24 hours of the amount ofcabazitaxel used to prepare the composition.

In some embodiments, when the composition consisting essentially ofcabazitaxel and HSA as described herein (e.g., sterile solid powder) isdissolved in an aqueous solvent (e.g., water, 0.9% saline or 5%dextrose), the resultant aqueous solution, when filtered using a 0.22micron filter, comprises at least 95% at the time of preparation, atleast 95% after 1 hour, at least 95% after 2 hours, at least 95% after 3hours, at least 95% after 4 hours, at least 95% after 5 hours, at least95% after 6 hours, or at least 95% after 24 hours of the amount ofcabazitaxel used to prepare the composition.

In some embodiments, the aqueous formulation is a clear aqueous solutionfor at least 1 hour. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 2 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 4 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 5 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours. Insome embodiments, the aqueous formulation is a clear aqueous solutionfor at least 8 hours. In some embodiments, the aqueous formulation is aclear aqueous solution for at least 24 hours. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 6 hours ata concentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is a clear aqueous solution for at least 24 hours. In someembodiments, the aqueous formulation is a transparent aqueous solutionfor at least 24 hours at a concentration of from about 5 mg/mL to about250 mg/mL, from about 10 mg/mL to about 200 mg/mL, from about 25 mg/mLto about 150 mg/mL, from about 10 mg/mL to about 50 mg/mL, from about 50mg/mL to about 100 mg/mL, from about 100 mg/mL to about 150 mg/mL, fromabout 150 mg/mL to about 200 mg/mL, or about 5 mg/mL, about 10 mg/mL,about 20 mg/mL, about 30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60mg/mL, about 70 mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100mg/mL at a temperature from about 1° C. to about 35° C., about 1° C. toabout 10° C., about 10° C. to about 20° C., about 20° C. to about 35°C., or about 1° C., about 5° C., about 10° C., about 15° C., about 20°C., about 25° C., about 30° C., or about 35° C. In some embodiments, theaqueous formulation is a clear aqueous solution for at least 3 days. Insome embodiments, the aqueous formulation is a transparent aqueoussolution for at least 3 days when dissolved in an aqueous solution at aconcentration of from about 5 mg/mL to about 250 mg/mL, from about 10mg/mL to about 200 mg/mL, from about 25 mg/mL to about 150 mg/mL, fromabout 10 mg/mL to about 50 mg/mL, from about 50 mg/mL to about 100mg/mL, from about 100 mg/mL to about 150 mg/mL, from about 150 mg/mL toabout 200 mg/mL, or about 5 mg/mL, about 10 mg/mL, about 20 mg/mL, about30 mg/mL, about 40 mg/mL, about 50 mg/mL, about 60 mg/mL, about 70mg/mL, about 80 mg/mL, about 90 mg/mL, or about 100 mg/mL at atemperature from about 1° C. to about 35° C., about 1° C. to about 10°C., about 10° C. to about 20° C., about 20° C. to about 35° C., or about1° C., about 5° C., about 10° C., about 15° C., about 20° C., about 25°C., about 30° C., or about 35° C. In some embodiments, the aqueousformulation is substantially free of solvent other than water. In someembodiments, the aqueous formulation is free of solvent other thanwater.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 96% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 97% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 98% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someembodiments, after the aqueous formulation is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 99% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration. In some embodiments, after the aqueousformulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 99.5% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some aspects of these embodiments, the aqueousformulation is filtered by a 0.22-micron filter at a time periodselected from 1 hour, 2 hours, 3, hours, 4 hours, 5 hours, 6 hours, 8hours, 12 hours, 18 hours and 24 hours. In some embodiments, the aqueousformulation is free of solvent other than water. In some embodiments,the aqueous formulation is substantially free of solvent other thanwater.

In some embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is substantially freeof solvent other than water. In some embodiments, after the aqueousformulation (e.g. a clear aqueous solution) is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 96%, 97%, 98%, 99%, or 99.5% of the total amount of cabazitaxel inthe aqueous solution before filtration, wherein the clear aqueoussolution has pH value from about 6 to about 7.5, and wherein the clearaqueous solution is substantially free of solvent other than water. Insome embodiments, after the aqueous formulation (e.g. a clear aqueoussolution) is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 96%, 97%, 98%, 99%, or99.5% of the total amount of cabazitaxel in the aqueous solution beforefiltration, wherein the clear aqueous solution has pH value from about 5to about 8, and wherein the clear aqueous solution is free of solventother than water. In some embodiments, after the aqueous formulation(e.g. a clear aqueous solution) is filtered by a 0.22 micron filter, theamount of cabazitaxel in the filtered aqueous solution is at least 96%,97%, 98%, 99%, or 99.5% of the total amount of cabazitaxel in theaqueous solution before filtration, wherein the clear aqueous solutionhas pH value from about 6 to about 7.5, and wherein the clear aqueoussolution is free of solvent other than water. In some aspects of theseembodiments, the aqueous formulation is filtered by a 0.22-micron filterat a time period selected from 1 hour, 2 hours, 3, hours, 4 hours, 5hours, 6 hours, 8 hours, 12 hours, 18 hours and 24 hours.

In some embodiments, after the aqueous formulation is filtered by a 0.22micron filter, the amount of cabazitaxel in the filtered aqueoussolution is at least 80% of the total amount of cabazitaxel in theaqueous solution before the filtration. In some embodiments, after theaqueous formulation is filtered by a 0.22 micron filter, the amount ofcabazitaxel in the filtered aqueous solution is at least 85% of thetotal amount of cabazitaxel in the aqueous solution before thefiltration. In some embodiments, after the aqueous formulation isfiltered by a 0.22 micron filter, the amount of cabazitaxel in thefiltered aqueous solution is at least 90% of the total amount ofcabazitaxel in the aqueous solution before the filtration. In someaspects of these embodiments, the aqueous formulation is filtered by a0.22-micron filter at a time period selected from 1 hour, 2 hours, 3,hours, 4 hours, 5 hours, 6 hours, 8 hours, 12 hours, 18 hours and 24hours. In some embodiments, the aqueous formulation is free of solventother than water. In some embodiments, the aqueous formulation issubstantially free of solvent other than water.

Also, provided herein is a pharmaceutical composition comprising thecomposition consisting essentially of the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

In some embodiments, the pharmaceutical composition further comprises atleast one anti-cancer drug (e.g., any one of the anti-cancer drugs asdescribed herein).

In some embodiments, the pharmaceutical composition is free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the pharmaceutical composition is substantially free of asurfactant, such as CREMOPHOR® surfactants and Polysorbate 80. In someembodiments, the pharmaceutical composition can be substantially free ofa surfactant selected from the group consisting of CREMOPHOR®surfactants and Polysorbate 80.

Also, provided herein is a method of treating a proliferative diseasecomprising the step of administering to a subject in need thereof apharmaceutical composition comprising the composition consistingessentially of the cabazitaxel and the human serum albumin as describedherein, and a pharmaceutically acceptable carrier.

Also, provided herein is a method of treating a cancer (e.g., any one ofcancers described herein), the method comprising the step ofadministering to a subject in need thereof of a therapeuticallyeffective amount of a pharmaceutical composition comprising thecomposition consisting essentially of the cabazitaxel and the humanserum albumin as described herein, and a pharmaceutically acceptablecarrier.

In some embodiments, the cancer is a solid tumor cancer. In someembodiments, the cancer is a prostate cancer.

In some embodiments, the method of treating a prostate cancer comprisesthe step of administering to a subject in need thereof of atherapeutically effective amount of a pharmaceutical compositioncomprising the composition consisting essentially of the cabazitaxel andthe human serum albumin as described herein, prednisone, and apharmaceutically acceptable carrier.

In some embodiments, the method of treating cancer (e.g., any one ofcancers described herein) comprises the step of administering to asubject in need thereof a therapeutically effective amount of apharmaceutical composition comprising the composition consistingessentially of the cabazitaxel and the human serum albumin as describedherein, and a therapeutically effective amount of at least one inhibitorof the kinases for the treatment of cancer described herein.

In some embodiments, the method of treating cancer (e.g. any one ofcancers described herein) comprises the step of administering to asubject in need thereof a therapeutically effective amount of apharmaceutical composition comprising the composition consistingessentially of the cabazitaxel and the human serum albumin as describedherein, and a therapeutically effective amount of at least oneanti-cancer drug described herein.

In some embodiments, a composition consisting essentially of thecabazitaxel and the human serum albumin as described herein and ananti-cancer drug are administered simultaneously.

In some embodiments, a composition consisting essentially of thecabazitaxel and the human serum albumin as described herein and ananti-cancer drug are administered consecutively.

The compositions consisting essentially of the cabazitaxel and the humanserum albumin described herein can be administered to an individual,such as human, via various routes, such as parenterally, includingintravenous, intra-arterial, intraperitoneal, intrapulmonary, oral,inhalation, intravesicular, intramuscular, intra-tracheal, subcutaneous,intraocular, intrathecal, or transdermal. For example, the compositioncan be administered by inhalation to treat conditions of the respiratorytract. The composition can be used to treat respiratory conditions suchas pulmonary fibrosis, broncheolitis obliterans, lung cancer,bronchoalveolar carcinoma, and the like. In some embodiments, thecomposition is administrated intravenously.

The methods described herein may be performed alone or in conjunctionwith another therapy, such as surgery, radiation, chemotherapy,immunotherapy, gene therapy, and the like. Additionally, a person havinga greater risk of developing the proliferative disease may receivetreatments to inhibit or and/or delay the development of the disease.

As will be understood by those of ordinary skill in the art, theappropriate doses of cabazitaxel will be approximately those alreadyemployed in clinical therapies wherein cabazitaxel is administered aloneor in combination with other chemotherapeutic agents. Variation indosage will likely occur depending on the condition being treated.Appropriate effective doses will also vary, as recognized by thoseskilled in the art, depending on the severity of the disease, the routeof administration, the sex, age and general health condition of thesubject, excipient usage, the possibility of co-usage with othertherapeutic treatments such as use of other agents, and the judgment ofthe treating physician. For example, guidance for selecting an effectivedose can be determined by reference to the prescribing information forcabazitaxel.

Methods of Making

Also, provided herein are several methods to prepare a compositioncomprising non-covalently bound complexes comprising the cabazitaxel andthe human serum albumin as described herein, a composition comprisingthe cabazitaxel and the human serum albumin as described herein, or acomposition consisting essentially of the cabazitaxel and the humanserum albumin as described herein.

In some embodiments, the method comprises the steps of:

(i) obtaining an organic solution of cabazitaxel in a polarwater-miscible organic solvent;

(ii) obtaining a first aqueous solution of human serum albumin; and

(iii) mixing the organic solution of cabazitaxel and the first aqueoussolution of human serum albumin to obtain a second aqueous solutioncomprising the composition comprising cabazitaxel and human serumalbumin as described herein.

A non-limiting embodiments of the disclosed methods are as follows.

Formation of the Organic Solution

Cabazitaxel is dissolved in a polar organic solvent (e.g., an alcoholsuch as methanol, ethanol, isopropanol, and/or n-butanol; THF, CH₃CN;DMF; or mixtures thereof) to form an organic solution.

As used herein, the term “organic solution” refers to a solution whereinat least one solvent is a non-aqueous solvent and the weight % of thenon-aqueous solvent in the mixture of solvents is at least 50%, at least60%, at least 70% or at least 90%. In some embodiments, organic solutionis a solution in which does not comprise water as a solvent.

In some embodiments, the terms “organic solvent” and “non-aqueoussolvent” are used interchangeably and refer to a liquid comprising is atleast 50%, at least 60%, at least 70%, at least 90%, or at least 95% ofa solvent other than water.

The polar organic solvent is miscible in water. In some embodiments, thepolar organic solvent is an alcohol. In some embodiments, the polarorganic solvent is ethanol or methanol, or mixtures thereof. Forexample, the polar organic solvent can be ethanol. In some embodiments,the polar organic solvent is methanol.

In some embodiments, the amount of polar organic solvent is from about0.05 mL to about 50 mL per mg of cabazitaxel. In some embodiments, theamount of polar organic solvent is from about 0.1 mL to about 20 mL permg of cabazitaxel. In some embodiments, the amount of polar organicsolvent is from about 0.5 mL to about 10 mL per mg of cabazitaxel. Insome embodiments, the amount of polar organic solvent is from about 1 mLto about 5 mL per mg of cabazitaxel. In some embodiments, theconcentration of cabazitaxel in the polar organic solvent is from about0.1 mM to about 5 mM, from about 0.1 mM to about 2 mM, from about 0.1 mMto about 1 mM, or from about 0.2 mM to about 1 mM.

Formation of the First Aqueous Solution

A defined amount of human serum albumin is dissolved in an amount ofaqueous solvent (e.g., any one of aqueous solvents described herein suchas water, 0.9% saline or 5% dextrose) to form a first aqueous solution.

In some embodiments, the amount of aqueous solvent (e.g., water) toprepare the first aqueous solution is from about 1 mL to about 10000 L,from about 2 mL to about 1000 L, from about 3 mL to about 100 L, fromabout 4 mL to about 10 L, from about 5 mL to about 2 L, from about 6 mLto about 1 L.

In some embodiments, the amount of HSA prepare the first aqueoussolution is from about 100 mg to about 1000 kg, from about 150 mg toabout 1000 kg, from about 200 mg to about 100 kg, from about 300 mg toabout 5 kg, from about 200 mg to about 500 g, or from about 200 mg toabout 100 g.

In some embodiments, the amount of aqueous solvent in the first aqueoussolution is from about 0.005 mL to about 10 mL per 1 mg of human serumalbumin. In some embodiments, the amount of aqueous solvent in the firstaqueous solution is from about 0.01 mL to about 5 mL per 1 mg of humanserum albumin. In some embodiments, the amount of aqueous solvent in thefirst aqueous solution is from about 0.01 mL to about 1 mL per 1 mg ofhuman serum albumin. In some embodiments, the amount of aqueous solventin the first aqueous solution is from about 0.01 mL to about 0.5 mL per1 mg of human serum albumin. In some embodiments, the amount of aqueoussolvent in the first aqueous solution is from about 0.01 mL to about 0.1mL per 1 mg of human serum albumin. In some embodiments, the amount ofaqueous solvent in the first aqueous solution is from about 0.01 mL toabout 0.05 mL per 1 mg of human serum albumin. In some embodiments, theamount of aqueous solvent in the first aqueous solution is from about0.01 mL to about 0.025 mL per 1 mg of human serum albumin. In someembodiments, the amount of aqueous solvent in the first aqueous solutionis from about 0.013 mL to about 0.022 mL per 1 mg of human serumalbumin. In some embodiments, the amount of aqueous solvent in the firstaqueous solution is from about 0.015 mL to about 0.04 mL per 1 mg ofhuman serum albumin. In some embodiments, the amount of aqueous solventin the first aqueous solution is about 0.007 mL, about 0.01 mL, about0.015 mL, about 0.02 mL, about 0.025 mL, about 0.03 mL, about 0.035 mL,about 0.04 mL, about 0.045 mL, or about 0.05 mL per 1 mg of human serumalbumin. In some embodiments, the amount of aqueous solvent in the firstaqueous solution is about 0.02 mL per 1 mg of human serum albumin. Insome embodiments, the amount of aqueous solvent (e.g., water) to preparethe first aqueous solution is from about or from about 0.005 mL to about1 mL, from about 0.015 mL to about 0.5 mL, from about 0.015 mL to about0.2 mL, from about 0.015 mL to about 0.1 mL, or from about 0.015 mL toabout 0.05 mL per 1 mg of HSA. In some embodiments, the amount ofaqueous solvent (e.g., water) to prepare the first aqueous solution isabout 0.01 mL, about 0.011 mL, about 0.012 mL, about 0.013 mL, about0.015 mL, about 0.017 mL, about 0.018 mL, about 0.019 mL about 0.02 mL,about 0.021 mL, about 0.022 mL, about 0.023 mL, about 0.024 mL, about0.025 mL, about 0.026 mL, about 0.027 mL, about 0.028 mL, about 0.029 mLor about 0.03 mL per 1 mg of HSA.

In some embodiments, the amount of HSA in the first aqueous solution isfrom about 10% w/w to about 25% w/w, or from about 13% w/w to about 22%w/w. In some embodiments, the amount of HSA in the first aqueoussolution is about 10% w/w, about 11% w/w, about 12% w/w, about 13% w/w,about 14% w/w, about 15% w/w, about 16% w/w, about 17% w/w, about 18%w/w, about 19% w/w, about 20% w/w, about 21% w/w, about 22% w/w, about23% w/w, about 24% w/w or about 25% w/w. In some embodiments, thepreparation of the organic solution and the preparation of the firstaqueous solution are performed concurrently.

In some embodiments, the preparation of the organic solution and thepreparation of the first aqueous solution are performed sequentially. Insome embodiments, the preparation of the organic solution is performedbefore the preparation of the first aqueous solution. In someembodiments, the preparation of the first aqueous solution is performedbefore the preparation of the organic solution.

In some embodiments, the range of pH in the first aqueous solution isfrom about 3 to about 9, from about 4 to about 8, from about 5 to about7, from about 6 to about 7, from about 3 to about 5, from about 3 toabout 7, from about 4 to about 6, from about 5 to about 6, or from about6 to about 6.5. In some embodiments, the pH of the first aqueoussolution is about 4, about 5, about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7, about 7.5, or about 8.

Formation of the Second Aqueous Solution

The organic solution of cabazitaxel is mixed with the first aqueoussolution of human serum albumin to form a second aqueous solution. Insome embodiments, the second aqueous solution is a clear aqueoussolution with no precipitation of cabazitaxel.

In some embodiments, the volume ratio of the amount of aqueous solvent(e.g., water) to the amount of the polar organic solvent (e.g.,methanol) is in a range from about 1:1 to about 1000:1. In someembodiments, the volume ratio of the amount of aqueous solvent (e.g.,water) to the amount of the polar organic solvent (e.g., methanol) is ina range from about 1.5:1 to about 100:1. In some embodiments, the volumeratio of the amount of aqueous solvent (e.g., water) to the amount ofthe polar organic solvent (e.g., methanol) is in a range from about1.5:1 to about 20:1. In some embodiments, the volume ratio of the amountof aqueous solvent (e.g., water) to the amount of the polar organicsolvent (e.g., methanol) is in a range from about 1.5:1 to about 10:1.In some embodiments, the volume ratio of the amount of aqueous solvent(e.g., water) to the amount of the polar organic solvent (e.g.,methanol) is in a range from about 1:1 to about 10:1. In someembodiments, the volume ratio of the amount of aqueous solvent (e.g.,water) to the amount of the polar organic solvent (e.g., methanol) is ina range from about 1:1 to about 3:1. In some embodiments, the volumeratio of the amount of aqueous solvent (e.g., water) to the amount ofthe polar organic solvent (e.g., methanol) is about 1.5:1, about 2:1,about 2.2:1, about 2.3:1, about 2.4:1, about 2.5:1, about 3:1, about4:1, about 5:1, about 6:1, about 7:1, about 8:1, about 9:1, or about10:1.

In some embodiments, the organic solution is added to the first aqueoussolution to form a second aqueous solution. In some embodiments, theorganic solution is added dropwise to the first aqueous solution to forma second aqueous solution. In some embodiments, the first aqueoussolution is added to the organic solution to form a second aqueoussolution. In some embodiments, the mixing is performed with agitation.In some embodiments, the mixing is performed with stirring. In someembodiments, the mixing is performed with shaking.

In some embodiments, the addition is done at the temperature from about0° C. to about 35° C. In some embodiments, the addition is done at thetemperature from about 0° C. to about 25° C. In some embodiments, theaddition is done at the temperature from about 0° C. to about 10° C. Insome embodiments, the addition is done at the temperature about 0° C. Insome embodiments, the addition is done at the temperature about 5° C. Insome embodiments, the addition is done at the temperature about 10° C.In some embodiments, the addition is done at ambient temperature (e.g.,room temperature).

In some embodiments, the time of addition is in a range from about 0.1min to about 24 hours. In some embodiments, the time of addition is in arange from about 1 min to about 2 hour. In some embodiments, the time ofaddition is in a range from about 1 min to about 1 hour. In someembodiments, the time of addition is in a range from about 5 min toabout 30 min.

In some embodiments, the rate of addition of organic solution to thefirst aqueous solution is from about 0.01 mL/min to about 100 mL/min,from about 0.02 mL/min to about 50 mL/min, from about 0.05 mL/min toabout 20 mL/min, from about 1 mL/min to about 10 mL/min, or from about0.01 mL/min to about 10 mL/min, from about 0.01 mL/min to about 5mL/min, from about 0.01 mL/min to about 2 mL/min, from about 0.01 mL/minto about 1 mL/min, from about 0.01 mL/min to about 0.5 mL/min, or fromabout 0.01 mL/min to about 0.1 mL/min.

In some embodiments, the rate of addition of organic solution to thefirst aqueous solution is about 0.01 mL/min, 0.02 mL/min, 0.03 mL/min,0.04 mL/min, 0.05 mL/min, 0.1 mL/min, 0.2 mL/min, 0.3 mL/min, 0.5mL/min, 0.6 mL/min, 0.8 mL/min, 1 mL/min, 1.5 mL/min, 2 mL/min, 3mL/min, 5 mL/min or 10 mL/min.

In some embodiments, the range of pH in the second aqueous solution isfrom about 3 to about 9, from about 4 to about 8, from about 5 to about7, from about 6 to about 7, from about 3 to about 5, from about 3 toabout 7, from about 4 to about 6, from about 5 to about 6, or from about6 to about 6.5. In some embodiments, the pH of the second aqueoussolution is about 4, about 5, about 6, about 6.1, about 6.2, about 6.3,about 6.4, about 6.5, about 6.6, about 6.7, about 6.8, about 6.9, about7, about 7.5, or about 8.

Optionally, the solvents including both water and organic solvent areremoved from the second aqueous solution to provide a solid withoutremoval of organic solvent first. In some embodiments, the solvents areremoved under a vacuum. In some embodiments, the solvents are removedusing rotary evaporation. In some embodiments, the solvents are removedby lyophilization. In some embodiments, the second aqueous solution wasfiltered before removal of the solvents.

Removal of Organic Solvent

Upon completion of mixing of the organic solution with the first aqueoussolution to form the second aqueous solution, the polar organic solventis removed from the second aqueous solution.

In some embodiments, the polar organic solvent is removed under reducedpressure. In some embodiments, the polar organic solvent is removedusing rotary evaporation. In some embodiments, the polar organic solventis removed under a vacuum.

In some embodiments, the removal of the polar organic solvent yields atransparent aqueous solution.

Removal of Water from the Second Aqueous Solution

Upon removal of the organic solvent from the second aqueous solution,the water can be removed from the second aqueous solution to provide asolid.

In some embodiments, the second aqueous solution is filtered beforeremoval of water. For example, the second aqueous solution can befiltered by a 0.22 micron filter before removal of water.

As used herein, the term “micron” refers to a unit of measure of oneone-thousandth of a millimeter.

In some embodiments, the water is removed under a vacuum. In someembodiments, the water is removed using rotary evaporation. In someembodiments, the water is removed by lyophilization.

In some embodiments, the solvents including both water and organicsolvent are removed from the second aqueous solution simultaneously toprovide a solid composition. In some embodiments, the solvents areremoved under a vacuum. In some embodiments, the solvents are removedusing rotary evaporation. In some embodiments, the solvents are removedby lyophilization. In some embodiments, the second aqueous solution wasfiltered before removal of the solvents.

Reconstitution of the Solid

In some embodiments the solid composition comprising the cabazitaxel andthe human serum albumin (e.g., the solid composition prepared byremoving organic solvent from the second aqueous solution and removingwater from the second aqueous solution) is mixed with a water solution.In some embodiments, the water solution is a saline solution. In someembodiments, the water solution is a 5% dextrose water solution. In someembodiments, the mixing is the addition of the water solution to thesolid. In some embodiments, the mixing is the addition of the solid tothe water solution. In some embodiments, the mixing reconstitutes thesolid. In some embodiments, the mixing yields a clear aqueous solution.In some embodiments, the range of pH in the reconstituted solution isfrom about 5 to about 8, from about 5 to about 7, from about 6 to about7, from about 6.5 to about 7.5, from about 4 to about 6, or from about 6to about 6.5. In some embodiments, the pH of the reconstituted solutionis about 5, about 6, about 6.4, about 6.5, about 6.6, about 6.7, about6.8, about 6.9, about 7, about 7.1, about 7.5, or about 8.

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this disclosure belongs. Methods and materials aredescribed herein for use in the present disclosure; other suitablemethods and materials known in the art can also be used. The materials,methods, and examples are illustrative only and not intended to belimiting. All publications, patent applications, patents, and otherreferences mentioned herein are incorporated by reference in theirentirety. In case of conflict, the present specification, includingdefinitions, will control.

Composition Prepared by the Process

In some embodiments, the present disclosure provides a compositioncomprising cabazitaxel and human serum albumin, wherein a ratio byweight of cabazitaxel and the human serum albumin in the composition isfrom about 1:10 to about 1:3000, produced by a method comprising thesteps of:

(i) obtaining an organic solution of cabazitaxel in a polarwater-miscible organic solvent;

(ii) obtaining a first aqueous solution of human serum albumin; and

(iii) mixing the organic solution of cabazitaxel and the first aqueoussolution of human serum albumin to obtain a second aqueous solutioncomprising the composition comprising cabazitaxel and human serumalbumin.

In some embodiments, the range of pH in the first aqueous solution isfrom about 3 to about 9, from about 4 to about 8, from about 5 to about8, from about 5 to about 7, from about 6 to about 7, from about 3 toabout 5, from about 3 to about 7, from about 4 to about 6, or from about6 to about 6.5. In some embodiments, the pH of the first aqueoussolution is about 4, about 5, about 6, about 6.4, about 6.5, about 6.6,about 6.7, about 6.8, about 6.9, about 7, about 7.1, about 7.5, or about8.

In some embodiments, the range of pH in the second aqueous solution isfrom about 3 to about 9, from about 4 to about 8, from about 5 to about8, from about 5 to about 7, from about 6 to about 7, from about 3 toabout 5, from about 3 to about 7, from about 4 to about 6, or from about6 to about 6.5. In some embodiments, the pH of the second aqueoussolution is about 4, about 5, about 6, about 6.4, about 6.5, about 6.6,about 6.7, about 6.8, about 6.9, about 7, about 7.1, about 7.5, or about8.

In some embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:2000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:150 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:200 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:800. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:500. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:250 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:300 to about 1:400. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:1000. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:220 to about 1:600. Insome embodiments, the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight of about 1:200, 1:210, 1:220, about1:230, about 1:240, about 1:250, about 1:260, about 1:270, about 1:280,about 1:290, about 1:300, about 1:310, about 1:320, about 1:330, about1:340, about 1:350, about 1:360, about 1:370, about 1:380, about 1:390,about 1:400, about 1:450, about 1:460, about 1:500 or about 1:600.

In some embodiments, the present disclosure provides a compositioncomprising cabazitaxel and human serum albumin, wherein the weight ratioof cabazitaxel and the human serum albumin in the composition is fromabout 1:100 to about 1:3000, produced by a method comprising the stepsof:

(i) obtaining an organic solution of cabazitaxel in a polarwater-miscible organic solvent;

(ii) obtaining a first aqueous solution of human serum albumin; and

(iii) mixing the organic solution of cabazitaxel and the first aqueoussolution of human serum albumin to obtain a second aqueous solutioncomprising the composition comprising cabazitaxel and human serumalbumin.

In some embodiments, the range of pH in the first aqueous solution isfrom about 3 to about 9, from about 4 to about 8, from about 5 to about8, from about 5 to about 7, from about 6 to about 7, from about 3 toabout 5, from about 3 to about 7, from about 4 to about 6, or from about6 to about 6.5. In some embodiments, the pH of the first aqueoussolution is about 4, about 5, about 6, about 6.4, about 6.5, about 6.6,about 6.7, about 6.8, about 6.9, about 7, about 7.1, about 7.5, or about8.

In some embodiments, the range of pH in the second aqueous solution isfrom about 3 to about 9, from about 4 to about 8, from about 5 to about8, from about 5 to about 7, from about 6 to about 7, from about 3 toabout 5, from about 3 to about 7, from about 4 to about 6, or from about6 to about 6.5. In some embodiments, the pH of the second aqueoussolution is about 4, about 5, about 6, about 6.4, about 6.5, about 6.6,about 6.7, about 6.8, about 6.9, about 7, about 7.1, about 7.5, or about8.

In some embodiments, the cabazitaxel can be a pharmaceuticallyacceptable salt of cabazitaxel. In some embodiments, cabazitaxel can beany one of crystal forms, amorphous forms, solvates and hydrates asdescribed herein.

In some embodiments, the human serum albumin is essentially fatty acidfree.

In some embodiments, the composition comprises a non-covalently boundcomplex comprising cabazitaxel and human serum albumin.

In some embodiments, the amount of the polar water-miscible organicsolvent in the organic solution is from about 0.05 mL to about 50 mL per1 mg of cabazitaxel.

In some embodiments, the amount of the polar water-miscible organicsolvent in the organic solution is from about 0.1 mL to about 20 mL per1 mg of cabazitaxel.

In some embodiments, the amount of the polar water-miscible organicsolvent in the organic solution is from about 1 mL to about 5 mL per 1mg of cabazitaxel.

In some embodiments, the concentration of cabazitaxel in the polarwater-miscible organic solvent in the organic solution is from about 0.3mM to about 1 mM.

In some embodiments, the amount of aqueous solvent in the first aqueoussolution is from about 0.005 mL to about 0.05 mL per 1 mg of human serumalbumin.

In some embodiments, the amount of aqueous solvent in the first aqueoussolution is from about 0.01 mL to about 0.05 mL per 1 mg of human serumalbumin.

In some embodiments, the amount of aqueous solvent in the first aqueoussolution is from about 0.015 mL to about 0.04 mL per 1 mg of human serumalbumin.

In some embodiments, the amount of aqueous solvent in the first aqueoussolution is from about 0.01 mL to about 0.025 mL per 1 mg of human serumalbumin.

In some embodiments, the amount of aqueous solvent in the first aqueoussolution is from about 0.01 mL to about 10 mL per 1 mg of human serumalbumin. In some embodiments, the amount of aqueous solvent in the firstaqueous solution is from about 0.01 mL to about 5 mL per 1 mg of humanserum albumin. In some embodiments, the amount of aqueous solvent in thefirst aqueous solution is from about 0.01 mL to about 1 mL per 1 mg ofhuman serum albumin. In some embodiments, the amount of aqueous solventin the first aqueous solution is from about 0.01 mL to about 0.5 mL per1 mg of human serum albumin. In some embodiments, the amount of aqueoussolvent in the first aqueous solution is from about 0.01 mL to about 0.1mL per 1 mg of human serum albumin. In some embodiments, the amount ofaqueous solvent in the first aqueous solution is from about 0.01 mL toabout 0.05 mL per 1 mg of human serum albumin. In some embodiments, theamount of aqueous solvent in the first aqueous solution is from about0.015 mL to about 0.04 mL per 1 mg of human serum albumin. In someembodiments, the amount of aqueous solvent in the first aqueous solutionis about 0.01 mL, about 0.015 mL, about 0.02 mL, about 0.025 mL, about0.03 mL, about 0.035 mL, about 0.04 mL, about 0.045 mL, or about 0.05 mLper 1 mg of human serum albumin. In some embodiments, the amount ofaqueous solvent in the first aqueous solution about 0.02 mL per 1 mg ofhuman serum albumin.

In some embodiments, the polar water-miscible organic solvent is analcohol selected from the group consisting of methanol, ethanol,isopropanol, n-butanol, and mixtures thereof.

In some embodiments, the polar water-miscible organic solvent isselected from methanol, ethanol, and mixtures thereof.

In some embodiments, the polar water-miscible organic solvent ismethanol.

In some embodiments, the aqueous solvent is water.

In some embodiments, the mixing comprises adding the organic solution tothe first aqueous solution. In some embodiments, wherein the mixingcomprises adding the first aqueous solution to the organic solution. Insome embodiments, the adding is carried out dropwise. In someembodiments, the adding is carried out for a period of time from severalminutes to several hours. In some embodiments, the adding is carried outfor a period of time from 2 min to 24 hours. In some embodiments, theadding is carried out for a period of time from 2 min minutes to 12hours, from 2 min to 6 hours, from 3 min to 3 hours, from 2 min to 1hour, from 2 min to 30 min, or from 2 min to 25 min.

In some embodiments, the mixing is carried out at a temperature fromabout 0° C. to about 25° C. In some embodiments, mixing is carried outat ambient temperature (e.g., about 25° C.). In some embodiments, themixing is carried out at a temperature from about 0° C. to about 5° C.In some embodiments, the mixing is carried out at about 0° C. In someembodiments, the mixing is carried out at ambient temperature (e.g.,room temperature).

In some embodiments, the volume ratio of the amount of aqueous solventto the amount of the organic solvent in the second aqueous solution isin a range from about 2:1 to about 3:1 (e.g., from about 2.2:1 to about2.4:1).

In some embodiments, the volume ratio of the amount of aqueous solventto the amount of the organic solvent in the second aqueous solution isin a range from about 1:1 to about 1000:1. In some embodiments, thevolume ratio of the amount of aqueous solvent to the amount of theorganic solvent in the second aqueous solution is in a range from about1.5:1 to about 100:1. In some embodiments, the volume ratio of theamount of aqueous solvent to the amount of the organic solvent in thesecond aqueous solution is in a range from about 1.5:1 to about 20:1. Insome embodiments, the volume ratio of the amount of aqueous solvent tothe amount of the organic solvent in the second aqueous solution is in arange from about 1.5:1 to about 10:1. In some embodiments, the volumeratio of the amount of aqueous solvent to the amount of the organicsolvent in the second aqueous solution is in a range from about 2:1 toabout 10:1. In some embodiments, the volume ratio of the amount ofaqueous solvent to the amount of the organic solvent in the secondaqueous solution is about 1.5:1, about 2:1, about 2.2:1, about 2.3:1,about 2.4:1, about 2.5:1, about 3:1, about 4:1, about 5:1, about 6:1,about 7:1, about 8:1, about 9:1, or about 10:1. In some embodiments, theaqueous solvent is water. In some embodiments, the aqueous solvent iswater and the organic solvent is an alcohol. In some embodiments, theaqueous solvent is water and the organic solvent is methanol. In someembodiments, the aqueous solvent is water and the organic solvent ismethanol, and the volume ration of water to methanol is from about 2:1to about 2.5:1.

In some embodiments, the composition further comprises removing thepolar water-miscible organic solvent from the second aqueous solution toobtain a third aqueous solution comprising the composition comprisingcabazitaxel and human serum albumin. In some embodiments, thecomposition comprises removing aqueous solvent from the third aqueoussolution to obtain the composition comprising cabazitaxel and humanserum albumin.

In some embodiments, the composition further comprises removing theorganic solvent (e.g. methanol) and the aqueous solvent (e.g., water)from the second aqueous solution to obtain the composition comprisingcabazitaxel and human serum albumin.

In some embodiments, the removing as carried out in vacuum (e.g., usingthe rotovap). In some embodiments, the removing is carried out bylyophilization.

In some embodiments, the composition forms a clear aqueous solution whenthe composition is dissolved in an aqueous solvent, and wherein thesolubility of the composition in the aqueous solution is at least 10mg/mL.

In some embodiments, the composition is a solid formulation

In some embodiments, the composition is an aqueous formulation. In someembodiments, the aqueous formulation is substantially free of solventother than water. In some embodiments, the aqueous formulation is freeof a surfactant. In some embodiments, the surfactant is selected fromthe group consisting of CREMOPHOR® surfactants and Polysorbate 80. Insome embodiments, the aqueous formulation is a clear aqueous solution.In some embodiments, the aqueous formulation is a clear aqueous solutionfor at least 2 hours, at least 4 hours, at least 6 hours, at least 8hours, at least 24 hours, at least 48 hours, or at least 72 hours.

In some embodiments, the present disclosure provides a pharmaceuticalcomposition comprising the composition as prepared by a process asdescribed herein, and a pharmaceutically acceptable carrier.

In some embodiments, the present disclosure provides a method oftreating a cancer, the method comprising the step of administering to asubject in need thereof a therapeutically effective amount of thepharmaceutical composition as described herein.

In some embodiments, the cancer is a solid tumor. In some embodiments,the cancer is a prostate cancer.

EXAMPLES

HPLC Analysis:

The HPLC system used herein is a SHIMADZU LC-10AT vp series system,which consists of a SHIMADZU LC-10AT vp pump, a manual injector, aSHIMADZU CTO-10AS vp column oven, a SHIMADZU SPD-10A vp wavelengthdetector, and a SHIMADZU LC solution workstation. Waters XTERRA RP10column (4.6 mm×150 mm, 5 μm) is used as an analytical column. The columnoven temperature is 30° C. Mobile phase is composed of methanol andwater (70:30 v/v) and pumped at a flow rate of 1 ml/minute. The effluentis detected at a wavelength of 233 nm using a UV detector. The sampleinjection amount is 20 μl.

Example 1: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:300.

Cabazitaxel (4 mg) was dissolved in methanol (10 mL) in a flask to givea clear solution. HSA (1200 mg) (native fatty acid free human serumalbumin purchased from SeraCare Life Sciences, product code: HS-455-80,which contains fatty acids <0.2 mg/gm) was dissolved in 22 ml of waterin a round bottom flask. The methanol solution of cabazitaxel was addedslowly dropwise into the flask of the HSA solution with rapid stirring.Upon completion of the addition, a clear solution was obtained. Themethanol was removed under vacuum until the volume of the solution wasabout 20 mL to give a clear solution. The clear aqueous solution wasfiltered by a 0.22 micron aqueous phase filter. The resulting clearaqueous solution was lyophilized overnight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at room temperature.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 24 hours at room temperature. This clear aqueous solution staysclear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 3 days at room temperature.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at 4° C. This clearaqueous solution stays clear and is free of visible precipitation of theundissolved cabazitaxel when visually observed after 24 hours at 4° C.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 3 days at 4° C.

Example 2: Composition Comprising Cabazitaxel and Human Serum Albumin(Recombinant Human Serum Albumin)

The ratio by weight of cabazitaxel to recombinant human serum albuminprepared was about 1:300.

Cabazitaxel (2 mg) was dissolved in methanol (5 mL) in a flask to give aclear solution. Recombinant human serum albumin (600 mg) (fatty acidfree recombinant human serum albumin (no fatty acids detected) purchasedfrom Wuhan Healthgen Biotechnology Corp.) was dissolved in 12 mL ofwater in a round bottom flask. The methanol solution of cabazitaxel wasadded slowly dropwise into the flask of the recombinant human serumalbumin solution with rapid stirring. Upon completion of the addition, aclear solution was obtained. The methanol was removed under vacuum untilthe volume of the solution was about 10 mL to give a clear solution. Theclear aqueous solution was filtered by a 0.22 micron aqueous phasefilter. The resulting clear aqueous solution was lyophilized overnightto give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at room temperature.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 24 hours at room temperature. This clear aqueous solution staysclear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 3 days at room temperature.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is clear of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at 4° C. This clearaqueous solution stays clear and is free of visible precipitation of theundissolved cabazitaxel when visually observed after 24 hours at 4° C.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 3 days at 4° C.

Example 3: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:350.

Cabazitaxel (2 mg) was dissolved in methanol (6 mL) in a flask to give aclear solution. HSA (700 mg) (native fatty acid free human serum albuminpurchased from SeraCare Life Sciences, product code: HS-455-80, whichcontains fatty acids <0.2 mg/gm) was dissolved in 14 mL of water in around bottom flask. The methanol solution of cabazitaxel was addedslowly dropwise into the flask of the HSA solution with rapid stirring.Upon completion of the addition, a clear solution was obtained. Themethanol was removed under vacuum until the volume of the solution wasabout 12 mL to give a clear solution. The clear aqueous solution wasfiltered by a 0.22 micron aqueous phase filter. The resulting clearaqueous solution was lyophilized overnight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at room temperature.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 24 hours at room temperature. This clear aqueous solution staysclear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 3 days at room temperature.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at 4° C. This clearaqueous solution stays clear and is free of visible precipitation of theundissolved cabazitaxel when visually observed after 24 hours at 4° C.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 3 days at 4° C.

Example 4: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:250.

Cabazitaxel (2 mg) was dissolved in methanol (4.2 mL) in a flask to givea clear solution. HSA (500 mg) (native fatty acid free human serumalbumin purchased from SeraCare Life Sciences, product code: HS-455-80,which contains fatty acids <0.2 mg/gm) was dissolved in 10 mL of waterin a round bottom flask. The methanol solution of cabazitaxel was addedslowly dropwise into the flask of the HSA solution with rapid stirring.Upon completion of the addition, a clear solution was obtained. Themethanol was removed under vacuum until the volume of the solution wasabout 8-9 mL to give a clear solution. The clear aqueous solution wasfiltered by a 0.22 micron aqueous phase filter. The resulting clearaqueous solution was lyophilized overnight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at room temperature.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 24 hours at room temperature. This clear aqueous solution staysclear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 3 days at room temperature.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at 4° C. This clearaqueous solution stays clear and is free of visible precipitation of theundissolved cabazitaxel when visually observed after 24 hours at 4° C.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 3 days at 4° C.

Example 5: Composition Comprising Cabazitaxel and Human Serum Albumin(Recombinant Human Serum Albumin)

The ratio by weight of cabazitaxel to recombinant human serum albuminprepared was about 1:400.

Cabazitaxel (1 mg) was dissolved in methanol (3.4 mL) in a flask to givea clear solution. Recombinant human serum albumin (400 mg) (fatty acidfree recombinant human serum albumin (no fatty acids detected) purchasedfrom Wuhan Healthgen Biotechnology Corp.) was dissolved in 8 mL of waterin a round bottom flask. The methanol solution of cabazitaxel was addedslowly dropwise into the flask of the recombinant human serum albuminsolution with rapid stirring. Upon completion of the addition, a clearsolution was obtained. The methanol was removed under vacuum until thevolume of the solution was about 7 mL to give a clear solution. Theclear aqueous solution was filtered by a 0.22 micron aqueous phasefilter. The resulting clear aqueous solution was lyophilized overnightto give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible particles or precipitation of theundissolved cabazitaxel when visually observed after 6 hours at roomtemperature. This clear aqueous solution stays clear and is free ofvisible precipitation of the undissolved cabazitaxel when visuallyobserved after 24 hours at room temperature. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 3 days at room temperature.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at 4° C. This clearaqueous solution stays clear and is free of visible precipitation of theundissolved cabazitaxel when visually observed after 24 hours at 4° C.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 3 days at 4° C.

Example 6: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:600.

Cabazitaxel (1 mg) was dissolved in methanol (4.2 mL) in a flask to givea clear solution. HSA (600 mg) (native human serum albumin purchasedfrom Golden West Biologicals, Inc., catalog #: HA1000) was dissolved in10 mL of water in a round bottom flask. The methanol solution ofcabazitaxel was added slowly dropwise into the flask of the HSA solutionwith rapid stirring. Upon completion of the addition, a clear solutionwas obtained. The methanol was removed under vacuum until the volume ofthe solution was about 8-9 mL to give a clear solution. The clearaqueous solution was filtered by a 0.22 micron aqueous phase filter. Theresulting clear aqueous solution was lyophilized overnight to give awhite solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible particles or precipitation of theundissolved cabazitaxel when visually observed after 6 hours at roomtemperature. This clear aqueous solution stays clear and is free ofvisible precipitation of the undissolved cabazitaxel when visuallyobserved after 24 hours at room temperature. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 3 days at room temperature.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear aqueous solution. This clear aqueous solutionstays clear and is free of visible precipitation of the undissolvedcabazitaxel when visually observed after 6 hours at 4° C. This clearaqueous solution stays clear and is free of visible precipitation of theundissolved cabazitaxel when visually observed after 24 hours at 4° C.This clear aqueous solution stays clear and is free of visibleprecipitation of the undissolved cabazitaxel when visually observedafter 3 days at 4° C.

Example 7: Measure the Correlation Between HPLC Peak Area and theCabazitaxel Concentration

Methanol solutions of cabazitaxel in 8 different concentrations, 0.025mg/mL, 0.0375 mg/mL, 0.05 mg/mL. 0.075 mg/mL, 0.1 mg/mL, 0.15 mg/mL, 0.2mg/mL and 0.25 mg/mL, were prepared. The 8 cabazitaxel methanolsolutions were analyzed in HPLC. The peak area and concentration ofcabazitaxel were correlated using linear regression. The linearregression data is shown as below.

Y(peak area)=8680+2.854E7*X(concentration),R=0.99998,P<0.0001.

Example 8: Measure the Absorption of the Composition Comprising theCabazitaxel and HSA by the 0.22 Micron Aqueous Phase Filter in theFiltration

300 mg of the lyophilized powder from the example 1 (the ratio by weightof cabazitaxel to HSA is about 1:300) was dissolved in 6 mL of water toform a clear solution. To this clear aqueous solution, 1 mL solution wastaken out to give the solution F0; additional 1 mL solution was takenout and filtered by a 0.22 micron aqueous phase filter to give thesolution F1; additional 1 mL solution was taken out and filtered throughthe same 0.22 micron aqueous phase filter used for the solution F1 togive the solution F2; additional 1 mL solution was taken out andfiltered through the same 0.22 micron aqueous phase filter used for thesolutions F1 and F2 to give the solution F3; additional 1 mL solutionwas taken out and filtered by the same 0.22 micron aqueous phase filterused for the solutions F1, F2, and F3 to give the solution F4; andadditional 1 mL solution was taken out and filtered by the same 0.22micron aqueous phase filter used for the solutions F1, F2, F3, and F4 togive the solution F5;

To 200 μl of the solutions F0, F1, F2, F3, F4, and F5 were added 800 μlof acetonitrile. The mixtures were vortexed for seconds and thencentrifuged at 4,000 g for 5 minutes. The supernatants were removed andcollected followed by injection on HPLC. Based on the HPLC data, theconcentrations of the solutions of F0, F1, F2, F3, F4, and F5 have beencalculated and shown in the Table 1. The concentration of the solutionF1 is significantly lower than the concentration of the solution of F0,which indicated that the filter membrane absorption was very significantin the beginning. The concentrations of the follow-up solutions F2, F3,F4, and F5 were increasing, which indicated that the filter membraneabsorption became saturated.

TABLE 1 Solution Number Concentration (mg/mL) F0 0.1419 F1 0.1147 F20.1400 F3 0.1417 F4 0.1423 F5 0.1424

Example 9: Measure the Cabazitaxel Concentrations in the Clear AqueousSolutions Before and after the Filtration at 0 Hour, 6 Hours, 24 Hours,and 72 Hours

Cabazitaxel (20 mg) was dissolved in methanol (43 mL) in a flask to givea clear solution. HSA (6 g) (native fatty acid free human serum albuminpurchased from SeraCare Life Sciences, product code: HS-455-80, whichcontains fatty acids <0.2 mg/gm) was dissolved in 100 mL of water in around bottom flask. The methanol solution of cabazitaxel was addedslowly dropwise into the flask of the HSA solution at 0° C. withstirring. Upon completion of the addition, a clear solution wasobtained. The methanol was removed under vacuum to give a clearsolution. The clear aqueous solution was filtered by a 0.22 micronaqueous phase filter. The resulting clear aqueous solution waslyophilized overnight to give a white solid.

4 vials each with 300 mg of the lyophilized solid were added with 6 mLof water. After the lyophilized solid was dissolved in water, one vialwas used for the experiment immediately, and other 3 vials were keep inthe room temperature and used for the experiment in the 3 different timepoints, 6 hours, 24 hours, and 72 hours. For the vial used theimmediately, 1 mL of the solution was taken out from the 6 mLtransparent aqueous solution to give the solution CA-0-0h, and theremaining 5 mL of the solution was filtered by the same 0.22 micronaqueous phase filter at 1 mL at a time to give the solutions CA-1-0h,CA-2-0h, CA-3-0h, CA-4-0h, and CA-5-0h, similar to the method used inthe example 8. To 200 μl of the solutions CA-0-0h and CA-5-0h were added800 μl of acetonitrile separately. The mixtures were vortexed forseconds and then centrifuged at 4,000 g for 5 minutes. The supematantswere removed and collected followed by injection on HPLC. The sameprocedure was repeated 2 more times for each of solutions CA-0-0h andCA-5-0h. Based on the HPLC data, the concentrations of the solutions ofCA-0-0h, and CA-5-0h have been calculated and shown in the Table 2. At 0hour, the concentration of the clear aqueous solution after thefiltration was about 98.6% of the concentration of the clear aqueoussolution before the filtration.

TABLE 2 Concentration Average Concentration Solution Number (mg/mL)(mg/mL) CA-0-0 h-1 0.1461 0.1460 CA-0-0 h-2 0.1460 CA-0-0 h-3 0.1458CA-5-0 h-1 0.1438 0.1440 CA-5-0 h-1 0.1438 CA-5-0 h-1 0.1445

At 6 hours, the experiments were done for the second 6 mL of the clearaqueous solution using the same protocol as for the first 6 mL of thetransparent aqueous solution at 0 hour. Based on the HPLC data, theconcentrations of the solutions of CA-0-6h, and CA-5-6h have beencalculated and shown in the Table 3. At 6 hours, the concentration ofthe clear aqueous solution after the filtration was about 96.9% of theconcentration of the clear aqueous solution before the filtration.

TABLE 3 Concentration Average Concentration Solution Number (mg/mL)(mg/mL) CA-0-6 h-1 0.1480 0.1482 CA-0-6 h-2 0.1484 CA-0-6 h-3 0.1482CA-5-6 h-1 0.1434 0.1436 CA-5-6 h-1 0.1441 CA-5-6 h-1 0.1433

At 24 hours, the experiments were done for the third 6 mL of the clearaqueous solution using the same protocol as for the first 6 mL of thetransparent aqueous solution at 0 hour. Based on the HPLC data, theconcentrations of the solutions of CA-0-24h, and CA-5-24h have beencalculated and shown in the Table 4. At 24 hours, the concentration ofthe clear aqueous solution after the filtration was about 97.8% of theconcentration of the clear aqueous solution before the filtration.

TABLE 4 Concentration Average Concentration Solution Number (mg/mL)(mg/mL) CA-0-24 h-1 0.1436 0.1436 CA-0-24 h-2 0.1429 CA-0-24 h-3 0.1444CA-5-24 h-1 0.1406 0.1405 CA-5-24 h-1 0.1407 CA-5-24 h-1 0.1402

At 72 hours, the experiments were done for the 4th 6 mL of the clearaqueous solution using the same protocol as for the first 6 mL of thetransparent aqueous solution at 0 hour. Based on the HPLC data, theconcentrations of the solutions of CA-0-72h, and CA-5-72h have beencalculated and shown in the Table 5. At 72 hours, the concentration ofthe clear aqueous solution after the filtration was about 98.8% of theconcentration of the clear aqueous solution before the filtration.

TABLE 5 Concentration Average Concentration Solution Number (mg/mL)(mg/mL) CA-0-72 h-1 0.1447 0.1445 CA-0-72 h-2 0.1450 CA-0-72 h-3 0.1437CA-5-72 h-1 0.1429 0.1428 CA-5-72 h-1 0.1422 CA-5-72 h-1 0.1433

Example 10: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:220.

Cabazitaxel (2 mg) was dissolved in methanol (3.9 mL) in a glass vial togive a clear solution. HSA (440 mg) (native fatty acid free human serumalbumin purchased from SeraCare Life Sciences, product code: HS-455-80,which contains fatty acids <0.2 mg/gm) as a powder was dissolved in 9 mLof water in a round bottom flask. The methanol solution of cabazitaxelwas added slowly dropwise into the flask of the HSA solution with rapidstirring at 0° C. Upon completion of the addition, a clear solution wasobtained. Then, the methanol in the solution was removed under vacuum togive a clear solution. The resulting clear aqueous solution waslyophilized overnight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a cloudy solution.

Example 11: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:240.

Cabazitaxel (2 mg) was dissolved in methanol (3.9 mL) in a glass vial togive a clear solution. HSA (480 mg) (native fatty acid free human serumalbumin purchased from SeraCare Life Sciences, product code: HS-455-80,which contains fatty acids <0.2 mg/gm) as a powder was dissolved in 9 mLof water in a round bottom flask. The methanol solution of cabazitaxelwas added slowly dropwise into the flask of the HSA solution with rapidstirring at 0° C. Upon completion of the addition, a clear solution wasobtained. Then, the methanol in the solution was removed under vacuum togive a clear solution. The resulting clear aqueous solution waslyophilized overnight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear solution.

Example 12: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:400.

Cabazitaxel (1 mg) was dissolved in methanol (3.4 mL) in a vial to givea clear solution. A solution of HSA (400 mg, 2 mL) (20% human serumalbumin solution for infusion (product name: AlbuRx) from CSL Behring)was added into 6 mL of water to give a HSA solution (8 mL) in a roundbottom flask. The methanol solution of cabazitaxel was added slowlydropwise into the flask of the HSA solution with rapid stirring at 0° C.Upon completion of the addition, a clear solution was obtained. Then,the methanol in the solution was removed under vacuum to give a clearsolution. The resulting clear aqueous solution was lyophilized overnightto give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear solution. White precipitation was formed inthe solution in 2 hours.

Example 13: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:460.

Cabazitaxel (1 mg) was dissolved in methanol (3.9 mL) in a vial to givea clear solution. A solution of HSA (460 mg, 2.3 mL) (20% human serumalbumin solution for infusion (product name: AlbuRx) from CSL Behring)was added into 6.9 mL of water to give a HSA solution (9.2 mL) in around bottom flask. The methanol solution of cabazitaxel was addedslowly dropwise into the flask of the HSA solution with rapid stirringat 0° C. Upon completion of the addition, a clear solution was obtained.Then, the methanol in the solution was removed under vacuum to give aclear solution. The resulting clear aqueous solution was lyophilizedovernight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear solution. The clear aqueous solution stayedclear without precipitation after 24 hours.

Example 14: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:250.

Cabazitaxel (20 mg) was dissolved in methanol (28.3 mL) in a glass vialto give a clear solution. HSA (5 g) (native fatty acid free human serumalbumin purchased from SeraCare Life Sciences, product code: HS-455-80,which contains fatty acids <0.2 mg/gm) as a powder was dissolved in 66mL of water in a round bottom flask. The methanol solution ofcabazitaxel was added slowly dropwise into the flask of the HSA solutionwith rapid stirring at 0° C. Upon completion of the addition, a clearsolution was obtained. Then, the methanol in the solution was removedunder vacuum to give a clear solution. The clear aqueous solution wasfiltered by a 0.22 micron aqueous phase filter. The resulting clearaqueous solution was lyophilized overnight to give a white solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear solution.

Example 15: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:300.

Cabazitaxel (15 mg) was dissolved in methanol (25.7 mL) in a glass vialto give a clear solution. HSA (4.5 g) (native fatty acid free humanserum albumin purchased from SeraCare Life Sciences, product code:HS-455-80, which contains fatty acids <0.2 mg/gm) as a powder wasdissolved in 60 mL of water in a round bottom flask. The methanolsolution of cabazitaxel was added slowly dropwise into the flask of theHSA solution with rapid stirring at 0° C. Upon completion of theaddition, a clear solution was obtained. Then, the methanol in thesolution was removed under vacuum to give a clear solution. The clearaqueous solution was filtered by a 0.22 micron aqueous phase filter. Theresulting clear aqueous solution was lyophilized overnight to give awhite solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear solution.

Example 16: Composition Comprising Cabazitaxel and Human Serum Albumin(HSA)

The ratio by weight of cabazitaxel to HSA prepared was about 1:330.

Cabazitaxel (15 mg) was dissolved in methanol (28.3 mL) in a glass vialto give a clear solution. HSA (4.95 g) (native fatty acid free humanserum albumin purchased from SeraCare Life Sciences, product code:HS-455-80, which contains fatty acids <0.2 mg/gm) as a powder wasdissolved in 66 mL of water in a round bottom flask. The methanolsolution of cabazitaxel was added slowly dropwise into the flask of theHSA solution with rapid stirring at 0° C. Upon completion of theaddition, a clear solution was obtained. Then, the methanol in thesolution was removed under vacuum to give a clear solution. The clearaqueous solution was filtered by a 0.22 micron aqueous phase filter. Theresulting clear aqueous solution was lyophilized overnight to give awhite solid.

A sample of 100 mg of the lyophilized solid was reconstituted by adding2 mL water to give a clear solution.

Example 17: Measure pH Value of the Clear Aqueous Solution ofComposition Comprising Cabazitaxel and Human Serum Albumin (HSA)

250 mg of the lyophilized solid of the composition comprisingcabazitaxel and HSA (the ratio by weight about 1:330) from Example 16was dissolved in 10 mL of water to give a clear aqueous solution. Theclear aqueous solution was kept at about 25° C. and measured for pHvalue. The pH value of the clear aqueous solution is 6.87 (3measurements: 6.88, 6.87, and 6.86).

500 mg of the lyophilized solid of the composition comprisingcabazitaxel and HSA (the ratio by weight about 1:330) from Example 16was dissolved in 10 mL of water to give a clear aqueous solution. Theclear aqueous solution was kept at about 25° C. and measured for pHvalue. The pH value of the clear aqueous solution is 6.80 (3measurements: 6.80, 6.81, and 6.80).

250 mg of the lyophilized solid of the composition comprisingcabazitaxel and HSA (the ratio by weight about 1:330) from Example 16was dissolved in 10 mL of 0.9% saline solution, which had pH value about5.41, to give a clear aqueous solution. The clear aqueous solution waskept at about 25° C. and measured for pH value. The pH value of theclear aqueous solution is 6.76 (3 measurements: 6.76, 6.76, and 6.77).

250 mg of the lyophilized solid of the composition comprisingcabazitaxel and HSA (the ratio by weight about 1:330) from Example 16was dissolved in 10 mL of 5% dextrose solution, which had pH value about4.40, to give a clear aqueous solution. The clear aqueous solution waskept at about 25° C. and measured for pH value. The pH value of theclear aqueous solution is 6.79 (3 measurements: 6.78, 6.79, and 6.79).

Example 18: Measure pH Value of the Clear Aqueous Solution ofComposition Comprising Cabazitaxel and Human Serum Albumin (HSA)

500 mg of the lyophilized solid of the composition comprisingcabazitaxel and HSA (the ratio by weight about 1:250) from Example 14was dissolved in 10 mL of water to give a clear aqueous solution. Theclear aqueous solution was kept at about 25° C. and measured for pHvalue. The pH value of the clear aqueous solution is 6.76 (3measurements: 6.77, 6.76, and 6.74).

Example 19: Measure the Cabazitaxel Concentrations in the Clear AqueousSolutions Before and after the Filtration at 0 Hour, and after theFiltration at 1 Hour, 2 Hours, 3 Hours, 4 Hours, 5 Hours, 6 Hours, and24 Hours

2.5 g of the lyophilized solid of the composition comprising cabazitaxeland HSA (the ratio by weight about 1:330) from Example 16 was dissolvedin 50 mL of water to give a clear aqueous solution, which was kept atabout 20° C. Immediately after the lyophilized solid was dissolved inwater, 6 mL of the clear aqueous solution was taken out from the 50 mLsolution. Then 1 mL of the solution was taken out from the 6 mL clearaqueous solution to give the solution CA-0-0h, and the remaining 5 mL ofthe solution was filtered by the same 0.22 micron aqueous phase filterat 1 mL at a time to give the solutions CA-1-0h, CA-2-0h, CA-3-0h,CA-4-0h, and CA-5-0h. To 200 μl of the solutions CA-0-0h and CA-5-0hwere added 800 μl of acetonitrile separately. The mixtures were vortexedfor seconds and then centrifuged at 4,000 g for 5 minutes. Thesupernatants were removed and collected followed by injection on HPLC.The same procedure was repeated 2 more times for each of solutionsCA-0-0h and CA-5-0h. Based on the HPLC data and the measurement data ofExample 7, the cabazitaxel concentrations of the solutions of CA-0-0h,and CA-5-0h have been calculated and shown in the Table 6. At 0 hour,the cabazitaxel concentration of the clear aqueous solution after thefiltration was about 99.63% of the cabazitaxel concentration of theclear aqueous solution before the filtration.

TABLE 6 Cabazitaxel Average Cabazitaxel Solution Number Concentration(mg/mL) Concentration (mg/mL) CA-0-0h-1 0.1367 0.1366 CA-0-0h-2 0.1367CA-0-0h-3 0.1363 CA-5-0h-1 0.1357 0.1361 CA-5-0h-2 0.1365 CA-5-0h-30.1361

At 1 hour, 5 mL of the clear aqueous solution was taken out from theremaining 44 mL of the aqueous solution. Then 1 mL of the solution wastaken out from the 5 mL clear aqueous solution and filtered by a 0.22micron aqueous phase filter to give the solution CA-1-1h, and theremaining 4 mL of the solution was filtered by the same 0.22 micronaqueous phase filter at 1 mL at a time to give the solutions CA-2-1h,CA-3-1h, CA-4-1h, and CA-5-1h. To 200 μl of the solution CA-5-1h wasadded 800 μl of acetonitrile. The mixture was vortexed for seconds andthen centrifuged at 4,000 g for 5 minutes. The supernatant was removedand collected followed by injection on HPLC. The same procedure wasrepeated 2 more times for the solution CA-5-1h. Based on the HPLC dataand the measurement data of Example 7, the cabazitaxel concentrations ofthe solution CA-5-1h have been calculated and shown in the Table 7. At 1hour, the cabazitaxel concentration of the clear aqueous solution afterthe filtration was about 99.63% of the cabazitaxel concentration of theclear aqueous solution at 0 hour before the filtration.

TABLE 7 Cabazitaxel Average Cabazitaxel Solution Number Concentration(mg/mL) Concentration (mg/mL) CA-5-1h-1 0.1362 0.1361 CA-5-1h-2 0.1363CA-5-1h-3 0.1359

At 2 hours, 5 mL of the clear aqueous solution was taken out from theremaining 39 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 2 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-2h have beencalculated and shown in the Table 8. At 2 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 99.41% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 8 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-2h-1 0.1364 0.1358 CA-5-2h-2 0.1359CA-5-2h-3 0.1351

At 3 hours, 5 mL of the clear aqueous solution was taken out from theremaining 34 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 3 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-3h have beencalculated and shown in the Table 9. At 3 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.98% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 9 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-3h-1 0.1353 0.1352 CA-5-3h-2 0.1353CA-5-3h-3 0.1349

At 4 hours, 5 mL of the clear aqueous solution was taken out from theremaining 29 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 4 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-4h have beencalculated and shown in the Table 10. At 4 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.76% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 10 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-4h-1 0.1355 0.1349 CA-5-4h-2 0.1349CA-5-4h-3 0.1343

At 5 hours, 5 mL of the clear aqueous solution was taken out from theremaining 24 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 5 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution DC-5-5h have beencalculated and shown in the Table 11. At 5 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.24% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 11 cabazitaxel Concentration Average cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-5h-1 0.1347 0.1342 CA-5-5h-2 0.1341CA-5-5h-3 0.1337

At 6 hours, 5 mL of the clear aqueous solution was taken out from theremaining 19 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 6 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-6h have beencalculated and shown in the Table 12. At 6 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.46% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 12 cabazitaxel Concentration Average cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-6h-1 0.1347 0.1345 CA-5-6h-2 0.1347CA-5-6h-3 0.1341

At 24 hours, 5 mL of the clear aqueous solution was taken out from theremaining 14 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 24 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-24h have beencalculated and shown in the Table 13. At 24 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.83% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 13 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-24h-1 0.1353 0.1350 CA-5-24h-2 0.1352CA-5-24h-3 0.1345

Example 20: Measure the Cabazitaxel Concentrations in the Clear AqueousSolutions Before and after the Filtration at 0 Hour, and after theFiltration at 1 Hour, 2 Hours, 3 Hours, 4 Hours, 6 Hours, and 24 Hours

2.25 g of the lyophilized solid of the composition comprisingcabazitaxel and HSA (the ratio by weight about 1:300) from Example 15was dissolved in 45 mL of water to give a clear aqueous solution, whichwas kept at about 20° C. Immediately after the lyophilized solid wasdissolved in water, 6 mL of the clear aqueous solution was taken outfrom the 45 mL solution. Then 1 mL of the solution was taken out fromthe 6 mL clear aqueous solution to give the solution CA-0-0h, and theremaining 5 mL of the solution was filtered by the same 0.22 micronaqueous phase filter at 1 mL at a time to give the solutions CA-1-0h,CA-2-0h, CA-3-0h, CA-4-0h, and CA-5-0h. To 200 μl of the solutionsCA-0-0h and CA-5-0h were added 800 μl of acetonitrile separately. Themixtures were vortexed for seconds and then centrifuged at 4,000 g for 5minutes. The supernatants were removed and collected followed byinjection on HPLC. The same procedure was repeated 2 more times for eachof solutions CA-0-0h and CA-5-0h. Based on the HPLC data and themeasurement data of Example 7, the cabazitaxel concentrations of thesolutions of CA-0-0h, and CA-5-0h have been calculated and shown in theTable 14. At 0 hour, the cabazitaxel concentration of the clear aqueoussolution after the filtration was about 98.75% of the cabazitaxelconcentration of the clear aqueous solution before the filtration.

TABLE 14 Cabazitaxel Average Cabazitaxel Solution Number Concentration(mg/mL) Concentration (mg/mL) CA-0-0h-1 0.1514 0.1522 CA-0-0h-2 0.1527CA-0-0h-3 0.1526 CA-5-0h-1 0.1509 0.1503 CA-5-0h-2 0.1498 CA-5-0h-30.1503

At 1 hour, 5 mL of the clear aqueous solution was taken out from theremaining 39 mL of the aqueous solution. Then 1 mL of the solution wastaken out from the 5 mL clear aqueous solution and filtered by a 0.22micron aqueous phase filter to give the solution CA-1-1h, and theremaining 4 mL of the solution was filtered by the same 0.22 micronaqueous phase filter at 1 mL at a time to give the solutions CA-2-1h,CA-3-1h, CA-4-1h, and CA-5-1h. To 200 μl of the solution CA-5-1h wasadded 800 μl of acetonitrile. The mixture was vortexed for seconds andthen centrifuged at 4,000 g for 5 minutes. The supernatant was removedand collected followed by injection on HPLC. The same procedure wasrepeated 2 more times for the solution CA-5-1h. Based on the HPLC dataand the measurement data of Example 7, the cabazitaxel concentrations ofthe solution CA-5-1h have been calculated and shown in the Table 15. At1 hour, the cabazitaxel concentration of the clear aqueous solutionafter the filtration was about 97.77% of the cabazitaxel concentrationof the clear aqueous solution at 0 hour before the filtration.

TABLE 15 Cabazitaxel Average Cabazitaxel Solution Number Concentration(mg/mL) Concentration (mg/mL) CA-5-1h-1 0.1492 0.1488 CA-5-1h-2 0.1488CA-5-1h-3 0.1484

At 2 hours, 5 mL of the clear aqueous solution was taken out from theremaining 34 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 2 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-2h have beencalculated and shown in the Table 16. At 2 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.16% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 16 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-2h-1 0.1497 0.1494 CA-5-2h-2 0.1496CA-5-2h-3 0.1490

At 3 hours, 5 mL of the clear aqueous solution was taken out from theremaining 29 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 3 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-3h have beencalculated and shown in the Table 17. At 6 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 98.16% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 17 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-3h-1 0.1496 0.1494 CA-5-3h-2 0.1497CA-5-3h-3 0.1490

At 4 hours, 5 mL of the clear aqueous solution was taken out from theremaining 24 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 4 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-4h have beencalculated and shown in the Table 18. At 4 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 97.63% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 18 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-4h-1 0.1488 0.1486 CA-5-4h-2 0.1493CA-5-4h-3 0.1478

At 6 hours, 5 mL of the clear aqueous solution was taken out from theremaining 19 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 6 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-6h have beencalculated and shown in the Table 19. At 6 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 97.90% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 19 cabazitaxel Concentration Average cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-6h-1 0.1490 0.1490 CA-5-6h-2 0.1493CA-5-6h-3 0.1488

At 24 hours, 5 mL of the clear aqueous solution was taken out from theremaining 14 mL of the aqueous solution. The experiments were done forthe 5 mL of the clear aqueous solution taken out at 24 hours using thesame protocol as for the 5 mL of the clear aqueous solution taken out at1 hour. Based on the HPLC data and the measurement data of Example 7,the cabazitaxel concentrations of the solution CA-5-24h have beencalculated and shown in the Table 20. At 24 hours, the cabazitaxelconcentration of the clear aqueous solution after the filtration wasabout 97.63% of the cabazitaxel concentration of the clear aqueoussolution at 0 hour before the filtration.

TABLE 20 Cabazitaxel Concentration Average Cabazitaxel Solution Number(mg/mL) Concentration (mg/mL) CA-5-24h-1 0.1483 0.1486 CA-5-24h-2 0.1494CA-5-24h-3 0.1481

Other Embodiments

It is to be understood that while the invention has been described inconjunction with the detailed description thereof, the foregoingdescription is intended to illustrate and not limit the scope of theinvention, which is defined by the scope of the appended claims. Otheraspects, advantages, and modifications are within the scope of thefollowing claims.

1-63. (canceled)
 64. A composition comprising cabazitaxel and humanserum albumin, wherein the cabazitaxel and the human serum albumin inthe composition have a ratio by weight from about 1:150 to about 1:1000.65. The composition of claim 64, wherein the cabazitaxel and the humanserum albumin in the composition have a ratio by weight from about 1:200to about 1:600.
 66. The composition of claim 64, wherein the cabazitaxeland the human serum albumin in the composition have a ratio by weightfrom about 1:250 to about 1:500.
 67. The composition of claim 64,wherein the cabazitaxel and the human serum albumin in the compositionhave a ratio by weight from about 1:300 to about 1:400.
 68. Thecomposition of claim 64, wherein the cabazitaxel and the human serumalbumin in the composition are in a ratio by weight of about 1:340, orabout 1:350.
 69. The composition of claim 64, wherein the composition isa clear aqueous solution when the composition is dissolved in an aqueoussolvent, and wherein the aqueous solution is substantially free ofsolvent other than water.
 70. The composition of claim 64, wherein thecomposition is a clear aqueous solution when the composition isdissolved in an aqueous solvent, and wherein after the clear aqueoussolution is filtered by a 0.22 micron filter, the amount of cabazitaxelin the filtered aqueous solution is at least 96% of the total amount ofcabazitaxel in the aqueous solution before the filtration.
 71. Thecomposition of claim 64, wherein the composition is a clear aqueoussolution when the composition is dissolved in an aqueous solvent, andwherein after the clear aqueous solution is filtered by a 0.22 micronfilter, the amount of cabazitaxel in the filtered aqueous solution is atleast 98% of the total amount of cabazitaxel in the aqueous solutionbefore the filtration.
 72. The composition of claim 64, wherein thecomposition is a clear aqueous solution for at least 3 hours when thecomposition is dissolved in an aqueous solvent.
 73. The composition ofclaim 64, wherein the composition is a solid formulation.
 74. Thecomposition of claim 64, wherein the composition is an aqueousformulation.
 75. The composition of claim 74, wherein the aqueousformulation is a clear aqueous solution for at least 3 hours, andwherein the aqueous formulation is substantially free of solvent otherthan water.
 76. The composition of claim 74, wherein the aqueousformulation is a clear aqueous solution for at least 6 hours, andwherein the aqueous formulation is substantially free of solvent otherthan water.
 77. A composition comprising cabazitaxel and human serumalbumin, wherein the cabazitaxel and the human serum albumin in thecomposition have a ratio by weight from about 1:100 to about 1:2000,wherein the composition forms a clear aqueous solution when thecomposition is dissolved in an aqueous solution, and wherein thesolubility of the composition in the aqueous solution is at least 10mg/ml.
 78. The composition of claim 77, wherein the cabazitaxel and thehuman serum albumin in the composition have a ratio by weight from about1:250 to about 1:800.
 79. The composition of claim 77, wherein thecomposition has a solubility in an aqueous solution of about 20 mg/ml,about 30 mg/ml, about 40 mg/ml, about 50 mg/ml, 60 mg/ml, about 70mg/ml, about 80 mg/ml, about 90 mg/ml, or about 100 mg/ml.
 80. Thecomposition of claim 64, wherein the human serum albumin in thecomposition is a native human serum albumin.
 81. A pharmaceuticalcomposition comprising the composition of claim 64, and apharmaceutically acceptable carrier.
 82. A method of treating a cancer,the method comprising the step of administering to a subject in needthereof a therapeutically effective amount of the pharmaceuticalcomposition of claim
 81. 83. The method of claim 82, wherein the canceris a prostate cancer.